Allele Registry

Canonical Allele Identifier: PA127901

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV000019840

ClinVar Variation:

18196

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.Glu382Lys	CA127900 NM_000477.7:c.1144G>A