Canonical Allele Identifier: PA317136
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206740
ClinVar RCV Id: RCV000188835 RCV000500830
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Ser169Pro
CA317134
NM_001165963.4:c.505T>C