Canonical Allele Identifier: PA108541
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68668
ClinVar RCV Id: RCV000059548 RCV001854248
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Trp190Arg
CA285246
NM_001165963.4:c.568T>C
CA349075387
NM_001165963.4:c.568T>A