Canonical Allele Identifier: PA2826394714
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2690483
ClinVar RCV Id: RCV003491867

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243372.1:p.Glu177Lys
CA395478889
NM_001256443.2:c.529G>A