Canonical Allele Identifier: PA2827783543
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2703974
ClinVar RCV Id: RCV003589783

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Gly1590Arg
CA349071216
NM_001353957.2:c.4768G>C