Canonical Allele Identifier: PA303248
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189899
ClinVar RCV Id: RCV000180851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Ser103Ile
CA303246
NM_001165963.4:c.308G>T