Canonical Allele Identifier: PA2825360209
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 279927

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035233.1:p.Gly1593Arg
CA501168
NM_001040143.2:c.4777G>A
CA349036819
NM_001040143.2:c.4777G>C