Canonical Allele Identifier: PA2827786351
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68635
ClinVar RCV Id: RCV000059514 RCV000517134 RCV001296129
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Leu1486Ser
CA285177
NM_001353958.2:c.4457T>C