Canonical Allele Identifier: PA2827752110
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2810635
ClinVar RCV Id: RCV003754115

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Ala1015Thr
CA349060265
NM_001353948.2:c.3043G>A