Allele Registry

Canonical Allele Identifier: PA2499275188

Gene: RP2 HGNC NCBI

ClinVar RCV:

RCV001351195

ClinVar Variation:

1046617

HGVS (amino-acid)	Matching Registered Transcripts
NP_008846.2:p.Arg118Pro	CA413039373 NM_006915.3:c.353G>C