Allele Registry

Canonical Allele Identifier: PA1139750034

Gene: KCNQ2 HGNC NCBI

ClinVar RCV:

RCV001224717

ClinVar Variation:

952581

HGVS (amino-acid)	Matching Registered Transcripts
NP_742107.1:p.Thr114Ser	CA409656456 NM_172109.3:c.341C>G CA409656458 NM_172109.3:c.340A>T