Allele Registry

Canonical Allele Identifier: PA285796

Gene: PRRT2 HGNC NCBI

ClinVar RCV:

RCV000082646

RCV000224146

RCV001082873

RCV002274919

RCV002311740

RCV002505010

ClinVar Variation:

96494

HGVS (amino-acid)	Matching Registered Transcripts
NP_660282.2:p.Pro216Leu	CA285795 NM_145239.3:c.647C>T