Canonical Allele Identifier: PA226237
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 98669
ClinVar RCV Id: RCV000084973 RCV001315051 RCV003238719
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Lys153Arg
CA226236
NM_000322.5:c.458A>G