Canonical Allele Identifier: PA2827753618
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68543

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Ala1441Pro
CA284958
NM_001353948.2:c.4321G>C