Canonical Allele Identifier: PA1139673252
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 942510
ClinVar RCV Id: RCV001212513 RCV001250303 RCV001530282
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Leu130Pro
CA364137665
NM_000322.5:c.389T>C