Allele Registry

Canonical Allele Identifier: PA113666

Gene: RHAG HGNC NCBI

ClinVar RCV:

RCV000013935

ClinVar Variation:

13060

HGVS (amino-acid)	Matching Registered Transcripts
NP_000315.2:p.Gly279Glu	CA122828 NM_000324.3:c.836G>A