Canonical Allele Identifier: PA2827749002
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 190023
ClinVar RCV Id: RCV000180979
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Ala24Thr
CA303581
NM_001353948.2:c.70G>A