Allele Registry

Canonical Allele Identifier: PA127933

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV000019874

ClinVar Variation:

18214

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.Arg24Leu	CA127932 NM_000477.7:c.71G>T