Allele Registry

Canonical Allele Identifier: PA2826394460

Gene: PRRT2 HGNC NCBI

ClinVar Allele:

530240

ClinVar RCV:

RCV002234540

ClinVar Variation:

536488

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243371.1:p.Gly323Trp	CA7994632 NM_001256442.2:c.967G>T