Canonical Allele Identifier: PA1139673276
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 953805
ClinVar RCV Id: RCV001226150

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Met138Thr
CA364137615
NM_000322.5:c.413T>C