Canonical Allele Identifier: PA916036963
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 93656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Met900Thr
CA266846
NM_001353961.2:c.2699T>C