Canonical Allele Identifier: PA2827764889
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 12883

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Thr864Met
CA256587
NM_001353950.2:c.2591C>T