Canonical Allele Identifier: PA2826394367
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 589154
ClinVar Variation Id: 2723191
ClinVar RCV Id: RCV003595363

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243371.1:p.Gly258Arg
CA280410301
NM_001256442.2:c.772G>C
CA395479636
NM_001256442.2:c.772G>A