Allele Registry

Canonical Allele Identifier: PA127961

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV000019891

ClinVar Variation:

18230

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.Tyr164Cys	CA127960 NM_000477.7:c.491A>G