Canonical Allele Identifier: PA2826013132
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2035368
ClinVar RCV Id: RCV002877478
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Arg1294Ser
CA349053042
NM_001165964.3:c.3882A>T
CA349053043
NM_001165964.3:c.3882A>C