Allele Registry

Canonical Allele Identifier: PA916062516

Gene: KCNQ2 HGNC NCBI

ClinVar RCV:

RCV000416952

ClinVar Variation:

375518

HGVS (amino-acid)	Matching Registered Transcripts
NP_742107.1:p.Asp266Glu	CA16044334 NM_172109.3:c.798T>A CA409653383 NM_172109.3:c.798T>G