Canonical Allele Identifier: PA2827750255
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 929416

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Ala354Pro
CA349071368
NM_001353948.2:c.1060G>C