Canonical Allele Identifier: PA2825357981
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1342691
ClinVar RCV Id: RCV001847365
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035233.1:p.Val251Ala
CA349017949
NM_001040143.2:c.752T>C