Canonical Allele Identifier: PA2825355482
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2931669
ClinVar RCV Id: RCV003792691

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Met1128Val
CA349022038
NM_001040142.2:c.3382A>G