Canonical Allele Identifier: PA2829530137
Gene: KCNQ2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1320124
ClinVar RCV Id: RCV001775297

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004509.2:p.Trp236Arg
CA317459238
NM_004518.5:c.706T>C
CA409654062
NM_004518.5:c.706T>A