Canonical Allele Identifier: PA916036845
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206838

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Pro705Thr
CA317497
NM_001353961.2:c.2113C>A