Canonical Allele Identifier: PA2580509579
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2046903
ClinVar RCV Id: RCV002913967 RCV003427525
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660282.2:p.His232Gln
CA395479311
NM_145239.3:c.696C>A
CA395479312
NM_145239.3:c.696C>G