Canonical Allele Identifier: PA2825355750
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1678590
ClinVar RCV Id: RCV002225191
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Ile1232Thr
CA349027561
NM_001040142.2:c.3695T>C