Canonical Allele Identifier: PA288923
Gene: KCNQ2 HGNC NCBI

Linked Data

ClinVar Variation Id: 129332

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_742105.1:p.Val450Met
CA288922
NM_172107.3:c.1348G>A