Allele Registry

Canonical Allele Identifier: PA127897

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV000019838

ClinVar Variation:

18194

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.Glu345Lys	CA127896 NM_000477.7:c.1033G>A