Canonical Allele Identifier: PA2828475539
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1059086
ClinVar RCV Id: RCV001368305 RCV003490230
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Thr1240Ile
CA349027715
NM_001371247.1:c.3719C>T