Canonical Allele Identifier: PA226274
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 98689
ClinVar RCV Id: RCV000085000 RCV000504657 RCV001854491 RCV003888459
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Ser212Gly
CA226273
NM_000322.5:c.634A>G