Canonical Allele Identifier: PA2827778512
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 426348

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Val203Ile
CA1943471
NM_001353955.2:c.607G>A