Canonical Allele Identifier: PA2826394071
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2793355
ClinVar RCV Id: RCV003760093
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243371.1:p.Glu10Val
CA395477021
NM_001256442.2:c.29A>T