Canonical Allele Identifier: PA2826260861
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_001189364.1:p.Ile1993Val
CA317690
NM_001202435.3:c.5977A>G