Allele Registry

Canonical Allele Identifier: PA127917

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV000019857

RCV003556053

ClinVar Variation:

18204

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.Asp574Gly	CA127916 NM_000477.7:c.1721A>G