Allele Registry

Canonical Allele Identifier: PA127975

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV000019898

ClinVar Variation:

18237

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.Glu529Lys	CA127974 NM_000477.7:c.1585G>A