Canonical Allele Identifier: PA2826394401
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2828783
ClinVar RCV Id: RCV003758219
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243371.1:p.Ala289Asp
CA395480197
NM_001256442.2:c.866C>A