Allele Registry

Canonical Allele Identifier: PA127969

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV000019895

ClinVar Variation:

18234

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.Glu357Lys	CA127968 NM_000477.7:c.1069G>A