Canonical Allele Identifier: PA2827772207
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2959868
ClinVar RCV Id: RCV003812043
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Asp1947Asn
CA349063399
NM_001353951.2:c.5839G>A