Canonical Allele Identifier: PA226334
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 98722
ClinVar RCV Id: RCV000085036 RCV001462596 RCV001530276 RCV001250380 RCV001352968 RCV003888461
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Ile32Val
CA226333
NM_000322.5:c.94A>G