Allele Registry

Canonical Allele Identifier: PA127942

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV000019880

RCV001152821

ClinVar Variation:

18219

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.Asp518Asn	CA127941 NM_000477.7:c.1552G>A