Canonical Allele Identifier: PA2827750477
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189880
ClinVar RCV Id: RCV000180833

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Met400Lys
CA303192
NM_001353948.2:c.1199T>A