Canonical Allele Identifier: PA2827788825
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2034846

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Ser1202Ile
CA349055685
NM_001353960.2:c.3605G>T