Allele Registry

Canonical Allele Identifier: PA213351

Gene: RHAG HGNC NCBI

ClinVar RCV:

RCV000202426

ClinVar Variation:

218296

HGVS (amino-acid)	Matching Registered Transcripts
NP_000315.2:p.Ile61Arg	CA213350 NM_000324.3:c.182T>G