Allele Registry

Canonical Allele Identifier: PA315494

Gene: KCNQ2 HGNC NCBI

ClinVar RCV:

RCV000187922

ClinVar Variation:

205920

HGVS (amino-acid)	Matching Registered Transcripts
NP_742105.1:p.Arg581Leu	CA315492 NM_172107.3:c.1742G>T