Allele Registry

Canonical Allele Identifier: PA127940

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV000019879

ClinVar Variation:

18218

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.Glu106Lys	CA127939 NM_000477.7:c.316G>A