Canonical Allele Identifier: PA2827773907
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 658067

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Thr1199Met
CA1942910
NM_001353952.2:c.3596C>T