Canonical Allele Identifier: PA2826260799
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2014067
ClinVar RCV Id: RCV002861311
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Leu1931Ser
CA349063832
NM_001202435.3:c.5792T>C