Canonical Allele Identifier: PA2829676463
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 427057

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Gly1746Glu
CA349068318
NM_006920.6:c.5237G>A