Canonical Allele Identifier: PA2828473522
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2307995
ClinVar RCV Id: RCV002884267

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Gln3His
CA349009640
NM_001371247.1:c.9G>C
CA349009642
NM_001371247.1:c.9G>T