Canonical Allele Identifier: PA317681
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206884
ClinVar RCV Id: RCV001359104 RCV000678302
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Ile1961Thr
CA317678
NM_001165963.4:c.5882T>C