Canonical Allele Identifier: PA266094
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68562
ClinVar RCV Id: RCV000059437
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Phe1676Ser
CA266092
NM_006920.6:c.5027T>C