Canonical Allele Identifier: PA2580509457
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1718129
ClinVar RCV Id: RCV002296581
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660282.2:p.Glu107Lys
CA395478171
NM_145239.3:c.319G>A