Canonical Allele Identifier: PA2827790828
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 450573
ClinVar RCV Id: RCV000519145 RCV001497480
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Gln1123Glu
CA349063734
NM_001353961.2:c.3367C>G