Canonical Allele Identifier: PA916036503
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Pro1837Leu
CA317617
NM_001353948.2:c.5510C>T