Canonical Allele Identifier: PA2826394079
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2069874
ClinVar RCV Id: RCV002966701
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243371.1:p.Val14Ile
CA395477046
NM_001256442.2:c.40G>A