Allele Registry

Canonical Allele Identifier: PA127911

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV000019848

ClinVar Variation:

18201

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.Glu406Lys	CA127910 NM_000477.7:c.1216G>A