Canonical Allele Identifier: PA226278
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 98692
ClinVar RCV Id: RCV000085003 RCV001052017 RCV001074371 RCV001250308 RCV001542667
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Cys213Tyr
CA226277
NM_000322.5:c.638G>A