Canonical Allele Identifier: PA2827755962
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2751140
ClinVar RCV Id: RCV003589476
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Leu108Val
CA1943535
NM_001353949.2:c.322C>G