Canonical Allele Identifier: PA2829530249
Gene: KCNQ2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1001558
ClinVar RCV Id: RCV001297877
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004509.2:p.Leu252Phe
CA409653879
NM_004518.5:c.756G>T
CA409653882
NM_004518.5:c.756G>C