Canonical Allele Identifier: PA2827778471
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189904
ClinVar RCV Id: RCV000180856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Gly177Val
CA303263
NM_001353955.2:c.530G>T