Canonical Allele Identifier: PA226255
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 98678
ClinVar RCV Id: RCV000084986 RCV003888456
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Tyr184Ser
CA226254
NM_000322.5:c.551A>C