Allele Registry

Canonical Allele Identifier: PA645510128

Gene: PRPH2 HGNC NCBI

ClinVar RCV:

RCV000504827

RCV000787665

RCV001051123

RCV001074827

RCV001250285

RCV001530240

RCV002248741

ClinVar Variation:

437965

HGVS (amino-acid)	Matching Registered Transcripts
NP_000313.2:p.Gly208Asp	CA3808568 NM_000322.5:c.623G>A