Canonical Allele Identifier: PA108115
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_001159435.1:p.Phe1687Ser
CA266092
NM_001165963.4:c.5060T>C