Allele Registry

Canonical Allele Identifier: PA645448634

Gene: PRRT2 HGNC NCBI

ClinVar RCV:

RCV000368601

RCV000463630

RCV001249313

RCV001711857

RCV002401988

ClinVar Variation:

284592

HGVS (amino-acid)	Matching Registered Transcripts
NP_660282.2:p.Gly258Glu	CA7994585 NM_145239.3:c.773G>A