Canonical Allele Identifier: PA2825360112
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2943871
ClinVar RCV Id: RCV003803429 RCV003989864
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035233.1:p.Ile1541Met
CA349036308
NM_001040143.2:c.4623C>G