Canonical Allele Identifier: PA2827754981
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1065176
ClinVar RCV Id: RCV001375625
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Ile1770Phe
CA349068196
NM_001353948.2:c.5308A>T