Allele Registry

Canonical Allele Identifier: PA127971

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV000019896

ClinVar Variation:

18235

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.Glu400Gln	CA127970 NM_000477.7:c.1198G>C