Canonical Allele Identifier: PA295642
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 138982
ClinVar RCV Id: RCV000153886 RCV000457065 RCV002316404
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Ile1465Val
CA295639
NM_001165963.4:c.4393A>G