Allele Registry

Canonical Allele Identifier: PA127949

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV000019884

ClinVar Variation:

18223

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.Lys264Glu	CA127948 NM_000477.7:c.790A>G