Allele Registry

Canonical Allele Identifier: PA317034

Gene: PRRT2 HGNC NCBI

ClinVar RCV:

RCV000055990

RCV000791448

RCV001332952

RCV001719806

RCV002354247

ClinVar Variation:

65757

HGVS (amino-acid)	Matching Registered Transcripts
NP_660282.2:p.Pro216Arg	CA317033 NM_145239.3:c.647C>G