Allele Registry

Canonical Allele Identifier: PA170821

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV000144399

ClinVar Variation:

156315

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.Asp574Ala	CA170820 NM_000477.7:c.1721A>C