Canonical Allele Identifier: PA2826394167
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 941309
ClinVar RCV Id: RCV001211067

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243371.1:p.Ser90Gly
CA395477931
NM_001256442.2:c.268A>G