Canonical Allele Identifier: PA2580509393
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2069874
ClinVar RCV Id: RCV002966701
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660282.2:p.Val14Ile
CA395477046
NM_145239.3:c.40G>A