Canonical Allele Identifier: PA916036690
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 93647
ClinVar RCV Id: RCV000079579 RCV003753084
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Ala459Pro
CA221583
NM_001353961.2:c.1375G>C