Canonical Allele Identifier: PA2827767268
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68636
ClinVar RCV Id: RCV000059515 RCV000986874 RCV001513378
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Arg1564Cys
CA219777
NM_001353950.2:c.4690C>T