Allele Registry

Canonical Allele Identifier: PA127919

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV000019858

ClinVar Variation:

18205

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.Asp587Asn	CA127918 NM_000477.7:c.1759G>A