Canonical Allele Identifier: PA2828886842
Gene: KCNQ2 HGNC NCBI

Linked Data

ClinVar Variation Id: 999695
ClinVar RCV Id: RCV001295719

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369164.1:p.Ala433Val
CA9958466
NM_001382235.1:c.1298C>T