Canonical Allele Identifier: PA2826394569
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1053369
ClinVar RCV Id: RCV001361704
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243372.1:p.Pro48Leu
CA280409073
NM_001256443.2:c.143C>T