Allele Registry

Canonical Allele Identifier: PA127965

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV000019893

ClinVar Variation:

18232

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.Gln292Arg	CA127964 NM_000477.7:c.875A>G