Allele Registry

Canonical Allele Identifier: PA127885

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV000019829

RCV003659627

ClinVar Variation:

18188

2780805

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.His27Gln	CA99696945 NM_000477.7:c.81C>A CA99696949 NM_000477.7:c.81C>G