Canonical Allele Identifier: PA2829675680
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1717863
ClinVar RCV Id: RCV002297858

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Met1216Thr
CA349055771
NM_006920.6:c.3647T>C