Allele Registry

Canonical Allele Identifier: PA127887

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV000019830

ClinVar Variation:

18189

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.Arg138Gly	CA127886 NM_000477.7:c.412C>G