Canonical Allele Identifier: PA1139673349
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 867057
ClinVar RCV Id: RCV001075561 RCV001213778
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Leu159Arg
CA364137471
NM_000322.5:c.476T>G