Canonical Allele Identifier: PA2826394706
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1449898
ClinVar RCV Id: RCV002004712 RCV003418245
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243372.1:p.Glu169Gly
CA395478841
NM_001256443.2:c.506A>G