Canonical Allele Identifier: PA315378
Gene: KCNQ2 HGNC NCBI

Linked Data

ClinVar Variation Id: 205876
ClinVar RCV Id: RCV000187870
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_742105.1:p.Glu231Gly
CA315377
NM_172107.3:c.692A>G