Canonical Allele Identifier: PA174961
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 98691
ClinVar RCV Id: RCV000085002 RCV000149468 RCV000149469 RCV001854492
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Cys213Arg
CA174960
NM_000322.5:c.637T>C