Canonical Allele Identifier: PA2827750453
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1365578
ClinVar RCV Id: RCV001961854
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Ala395Val
CA1943338
NM_001353948.2:c.1184C>T