Canonical Allele Identifier: PA2827781197
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206887
ClinVar RCV Id: RCV000189029 RCV001206735 RCV003137765
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Ile1981Val
CA317690
NM_001353955.2:c.5941A>G