Canonical Allele Identifier: PA2827789838
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1523055
ClinVar RCV Id: RCV002048821

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Asp1775Asn
CA349067735
NM_001353960.2:c.5323G>A