Canonical Allele Identifier: PA2827773959
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68531

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Gly1222Arg
CA284928
NM_001353952.2:c.3664G>C