Allele Registry

Canonical Allele Identifier: PA127977

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV000019899

ClinVar Variation:

18238

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.Arg242Pro	CA127976 NM_000477.7:c.725G>C