Canonical Allele Identifier: PA1139673294
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 846922
ClinVar RCV Id: RCV001050346 RCV001161384 RCV001161386 RCV001162922 RCV001162924 RCV001161385 RCV001162923 RCV001530339 RCV003890189
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Met152Val
CA3808609
NM_000322.5:c.454A>G