Allele Registry

Canonical Allele Identifier: PA127907

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV000019846

RCV003556052

ClinVar Variation:

18199

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.Asp399Asn	CA127906 NM_000477.7:c.1195G>A