Canonical Allele Identifier: PA2741814471
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2767001
ClinVar RCV Id: RCV003592133
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Asn109Ser
CA364137795
NM_000322.5:c.326A>G