Allele Registry

Canonical Allele Identifier: PA2826394062

Gene: PRRT2 HGNC NCBI

ClinVar Variation Id: 1381913

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243371.1:p.Ser4Arg	CA7994460 NM_001256442.2:c.12C>A CA395476978 NM_001256442.2:c.10A>C CA395476984 NM_001256442.2:c.12C>G