Canonical Allele Identifier: PA2826394760
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65757

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243372.1:p.Pro216Arg
CA317033
NM_001256443.2:c.647C>G