Canonical Allele Identifier: PA2825359157
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1502099
ClinVar RCV Id: RCV002020066
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035233.1:p.Ser987Cys
CA349019480
NM_001040143.2:c.2959A>T