Canonical Allele Identifier: PA916036656
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 190031
ClinVar RCV Id: RCV000180987 RCV001035456
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Glu407Gln
CA303606
NM_001353961.2:c.1219G>C