Canonical Allele Identifier: PA2826394124
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1713442
ClinVar RCV Id: RCV002302927
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243371.1:p.Thr54Ser
CA395477523
NM_001256442.2:c.160A>T
CA395477526
NM_001256442.2:c.161C>G