Canonical Allele Identifier: PA2826394512
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2920091
ClinVar RCV Id: RCV003761169
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243372.1:p.Ser6Phe
CA395476996
NM_001256443.2:c.17C>T