Canonical Allele Identifier: PA2827752724
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1717863
ClinVar RCV Id: RCV002297858

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Met1227Thr
CA349055771
NM_001353948.2:c.3680T>C