Allele Registry

Canonical Allele Identifier: PA127954

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV000019887

ClinVar Variation:

18226

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.His27Tyr	CA127953 NM_000477.7:c.79C>T