Canonical Allele Identifier: PA2829530438
Gene: KCNQ2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1700189
ClinVar RCV Id: RCV002274438
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004509.2:p.Trp269Cys
CA409653355
NM_004518.5:c.807G>T
CA409653357
NM_004518.5:c.807G>C