Canonical Allele Identifier: PA645448602
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 373401
ClinVar RCV Id: RCV000413274 RCV000476515
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660282.2:p.Pro152His
CA16042942
NM_145239.3:c.455C>A