Canonical Allele Identifier: PA658659102
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 426348
ClinVar RCV Id: RCV000489802 RCV000545965 RCV002275035
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Val203Ile
CA1943471
NM_001165963.4:c.607G>A