Canonical Allele Identifier: PA317020
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 206683
ClinVar RCV Id: RCV000188762 RCV002228827
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660282.2:p.Ala139Thr
CA317019
NM_145239.3:c.415G>A