Canonical Allele Identifier: PA2826394339
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2792544
ClinVar RCV Id: RCV003760088
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243371.1:p.Ser238Cys
CA395479366
NM_001256442.2:c.713C>G