Canonical Allele Identifier: PA916076655
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 808028

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660282.2:p.Ala289Val
CA395480201
NM_145239.3:c.866C>T