Allele Registry

Canonical Allele Identifier: PA170809

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV000144392

ClinVar Variation:

156308

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.Asp399His	CA170808 NM_000477.7:c.1195G>C