Canonical Allele Identifier: PA2827756279
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 665186
ClinVar RCV Id: RCV000823411 RCV001585765 RCV002363173
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Ser213Leu
CA1943469
NM_001353949.2:c.638C>T