Canonical Allele Identifier: PA2573167111
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1358170
ClinVar RCV Id: RCV001894157
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Tyr140Cys
CA364137598
NM_000322.5:c.419A>G