Canonical Allele Identifier: PA2827790897
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1306292
ClinVar RCV Id: RCV001767245
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Lys1193Asn
CA349062884
NM_001353961.2:c.3579A>T
CA349062885
NM_001353961.2:c.3579A>C