Allele Registry

Canonical Allele Identifier: PA127891

Gene: ALB HGNC NCBI

ClinVar Allele:

33230

ClinVar RCV:

RCV000019833

ClinVar Variation:

18191

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.Asp293Gly	CA127890 NM_000477.7:c.878A>G