Canonical Allele Identifier: PA2827760850
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2703974
ClinVar RCV Id: RCV003589783
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Gly1607Arg
CA349071216
NM_001353949.2:c.4819G>C