Allele Registry

Canonical Allele Identifier: PA127956

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV000019888

RCV001153985

ClinVar Variation:

18227

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.Lys249Gln	CA127955 NM_000477.7:c.745A>C