Canonical Allele Identifier: PA2825359955
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1180106
ClinVar RCV Id: RCV001537239
ClinVar Variation Id: 1308640

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035233.1:p.Gln1479His
CA349034361
NM_001040143.2:c.4437G>C
CA349034362
NM_001040143.2:c.4437G>T