Canonical Allele Identifier: PA2827784138
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 971809
ClinVar RCV Id: RCV001247682
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Glu1929Gln
CA349063410
NM_001353957.2:c.5785G>C