Canonical Allele Identifier: PA2826394535
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2183022
ClinVar RCV Id: RCV002592314
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243372.1:p.Val20Ile
CA395477107
NM_001256443.2:c.58G>A