Canonical Allele Identifier: PA2827787100
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68671
ClinVar RCV Id: RCV000059551 RCV000416094 RCV000537890 RCV000764283 RCV002247465 RCV004019071
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Glu1929Gly
CA213190
NM_001353958.2:c.5786A>G