Canonical Allele Identifier: PA2573167104
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1364193
ClinVar RCV Id: RCV001905280

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Gly133Arg
CA3808622
NM_000322.5:c.397G>A
CA364137649
NM_000322.5:c.397G>C