Canonical Allele Identifier: PA2830346670
Gene: KCNQ2 HGNC NCBI

Linked Data

ClinVar Variation Id: 7389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_742106.1:p.Ser247Trp
CA130021
NM_172108.3:c.740C>G