Canonical Allele Identifier: PA2827783792
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1066554
ClinVar RCV Id: RCV001377574

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Asp1714Asn
CA1942685
NM_001353957.2:c.5140G>A