Canonical Allele Identifier: PA2826394525
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 767384
ClinVar RCV Id: RCV001395746

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243372.1:p.Gly13Arg
CA7994466
NM_001256443.2:c.37G>C
CA395477040
NM_001256443.2:c.37G>A