Allele Registry

Canonical Allele Identifier: PA2741814598

Gene: PRPH2 HGNC NCBI

ClinVar RCV:

RCV003757389

ClinVar Variation:

2796716

HGVS (amino-acid)	Matching Registered Transcripts
NP_000313.2:p.Gln304Lys	CA364133178 NM_000322.5:c.910C>A