Canonical Allele Identifier: PA2499231052
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1175238
ClinVar RCV Id: RCV001530270

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Arg13Gln
CA3808676
NM_000322.5:c.38G>A