Canonical Allele Identifier: PA315393
Gene: KCNQ2 HGNC NCBI

Linked Data

ClinVar Variation Id: 205881
ClinVar RCV Id: RCV000187876
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_742105.1:p.Trp269Leu
CA315392
NM_172107.3:c.806G>T