Canonical Allele Identifier: PA2826394073
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1062259
ClinVar RCV Id: RCV001371955
ClinVar Variation Id: 2174878
ClinVar RCV Id: RCV002588220
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243371.1:p.Met11Leu
CA7994465
NM_001256442.2:c.31A>T
CA395477024
NM_001256442.2:c.31A>C