Canonical Allele Identifier: PA2827750436
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2848903
ClinVar RCV Id: RCV003754688
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Arg393Gly
CA349071039
NM_001353948.2:c.1177C>G