Canonical Allele Identifier: PA916036711
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 663230
ClinVar RCV Id: RCV000821070
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Leu495Val
CA349053265
NM_001353961.2:c.1483C>G