Canonical Allele Identifier: PA2580114042
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2069820
ClinVar RCV Id: RCV002966658
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Asp157Gly
CA364137488
NM_000322.5:c.470A>G