Canonical Allele Identifier: PA2828474137
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2953829
ClinVar RCV Id: RCV003813052
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Thr365Arg
CA349020644
NM_001371247.1:c.1094C>G