Canonical Allele Identifier: PA2826013653
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68556

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Val1602Met
CA284988
NM_001165964.3:c.4804G>A