Canonical Allele Identifier: PA645472244
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 356777

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Ser217Gly
CA3808563
NM_000322.5:c.649A>G