Canonical Allele Identifier: PA2573071291
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1306292
ClinVar RCV Id: RCV001767245

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Lys2007Asn
CA349062884
NM_001353948.2:c.6021A>T
CA349062885
NM_001353948.2:c.6021A>C