Canonical Allele Identifier: PA2827782602
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 12890

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Leu958Phe
CA281911
NM_001353957.2:c.2872C>T