Allele Registry

Canonical Allele Identifier: PA1139673384

Gene: PRPH2 HGNC NCBI

ClinVar RCV:

RCV001074888

ClinVar Variation:

866675

HGVS (amino-acid)	Matching Registered Transcripts
NP_000313.2:p.Asp173Gly	CA364137382 NM_000322.5:c.518A>G