Allele Registry

Canonical Allele Identifier: PA288937

Gene: KCNQ2 HGNC NCBI

ClinVar Allele:

134789

ClinVar RCV:

RCV000117347

RCV000461909

RCV000678205

RCV000990327

ClinVar Variation:

129343

HGVS (amino-acid)	Matching Registered Transcripts
NP_742105.1:p.Arg871Ser	CA288935 NM_172107.3:c.2613G>T CA409636308 NM_172107.3:c.2613G>C