Canonical Allele Identifier: PA2826258001
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68597
ClinVar RCV Id: RCV000059474 RCV000819332 RCV003157390
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Ile91Thr
CA285081
NM_001202435.3:c.272T>C