Protein level identifier (NP_006740):
p.Pro568Leu
cDNA level identifier (NM_006749):
c.1703C>T
Gene level identifier:
g.109482C>T
Archive identifier/Other designation:
p.P568L
Reference, alternative allele:
G, A
Genomic location hg(19)
Gene name:
Consequence:
missense
Pathogenicity scoring:
Probably pathogenic
CADD score:
not available
Positive functional evidence:
not available
Number of all included cases:
1 heterozygous (1 in total).