Canonical Allele Identifier: PA2827785842
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1405896
ClinVar RCV Id: RCV001915567
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Ile1196Val
CA349055844
NM_001353958.2:c.3586A>G