Canonical Allele Identifier: PA2573167067
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1492157

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Ala2Thr
CA364138980
NM_000322.5:c.4G>A