Allele Registry

Canonical Allele Identifier: PA127952

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV000019886

RCV001753423

RCV003398549

ClinVar Variation:

18225

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.Arg242His	CA127951 NM_000477.7:c.725G>A