Canonical Allele Identifier: PA2827770669
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 12890

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Leu975Phe
CA281911
NM_001353951.2:c.2923C>T