Canonical Allele Identifier: PA2827760203
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1739737
ClinVar RCV Id: RCV002332074
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Asp1432His
CA349049553
NM_001353949.2:c.4294G>C