Allele Registry

Canonical Allele Identifier: PA127925

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV000019867

ClinVar Variation:

18208

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.Lys597Glu	CA127924 NM_000477.7:c.1789A>G