Canonical Allele Identifier: PA2828474135
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2435687
ClinVar RCV Id: RCV003136437 RCV004246054
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Thr365Met
CA349020645
NM_001371247.1:c.1094C>T