Canonical Allele Identifier: PA303195
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189880
ClinVar RCV Id: RCV000180833

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Met400Lys
CA303192
NM_006920.6:c.1199T>A