Canonical Allele Identifier: PA2826010215
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2035368
ClinVar RCV Id: RCV002877478

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Arg1322Ser
CA349053042
NM_001165963.4:c.3966A>T
CA349053043
NM_001165963.4:c.3966A>C