Canonical Allele Identifier: PA2826010070
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2313708
ClinVar RCV Id: RCV002905094 RCV003753257
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Thr1222Ile
CA349055889
NM_001165963.4:c.3665C>T