Canonical Allele Identifier: PA2826394170
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2908468
ClinVar RCV Id: RCV003760446
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243371.1:p.Gly92Glu
CA7994499
NM_001256442.2:c.275G>A