Allele Registry

Canonical Allele Identifier: PA127884

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV001796718

ClinVar Variation:

18187

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.Asp25Val	CA127883 NM_000477.7:c.74A>T