Canonical Allele Identifier: PA2827779159
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2251743
ClinVar RCV Id: RCV002772149
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Cys646Ser
CA349067243
NM_001353955.2:c.1937G>C
CA349067247
NM_001353955.2:c.1936T>A