Allele Registry

Canonical Allele Identifier: PA122935

Gene: PRPH2 HGNC NCBI

ClinVar RCV:

RCV000014055

RCV000084977

RCV001857348

ClinVar Variation:

13169

HGVS (amino-acid)	Matching Registered Transcripts
NP_000313.2:p.Gly167Asp	CA122934 NM_000322.5:c.500G>A