Canonical Allele Identifier: PA2827770428
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189957
ClinVar RCV Id: RCV000180911

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Glu835Gly
CA303403
NM_001353951.2:c.2504A>G