Canonical Allele Identifier: PA2830345790
Gene: KCNQ2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1700189
ClinVar RCV Id: RCV002274438

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_742105.1:p.Trp269Cys
CA409653355
NM_172107.3:c.807G>T
CA409653357
NM_172107.3:c.807G>C