Canonical Allele Identifier: PA2826011541
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_001159436.1:p.Ser169Pro
CA317134
NM_001165964.3:c.505T>C