Allele Registry

Canonical Allele Identifier: PA127938

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV000019878

ClinVar Variation:

18217

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.Glu84Lys	CA127937 NM_000477.7:c.250G>A