Canonical Allele Identifier: PA2826394786
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 536490
ClinVar RCV Id: RCV000644955
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243372.1:p.Gly237Arg
CA7994574
NM_001256443.2:c.709G>A
CA395479355
NM_001256443.2:c.709G>C