Allele Registry

Canonical Allele Identifier: PA113700

Gene: RHAG HGNC NCBI

ClinVar RCV:

RCV000490272

RCV002057061

RCV002485373

ClinVar Variation:

225454

HGVS (amino-acid)	Matching Registered Transcripts
NP_000315.2:p.Val270Ile	CA357863 NM_000324.3:c.808G>A