Canonical Allele Identifier: PA2826394469
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2765295
ClinVar RCV Id: RCV003594461

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243371.1:p.Leu326del
CA7994633
NM_001256442.2:c.976_978del