Canonical Allele Identifier: PA2827782207
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189900
ClinVar RCV Id: RCV000180852

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Trp710Leu
CA303250
NM_001353957.2:c.2129G>T