Canonical Allele Identifier: PA2827753095
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1385928
ClinVar RCV Id: RCV001889064
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Leu1318Val
CA349053111
NM_001353948.2:c.3952C>G