Canonical Allele Identifier: PA645422887
Gene: KCNQ2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405206
ClinVar RCV Id: RCV000464062

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_742105.1:p.Ser694Thr
CA9958157
NM_172107.3:c.2081G>C