Canonical Allele Identifier: PA2828473940
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 449164
ClinVar RCV Id: RCV000520182 RCV004017661 RCV001257708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Ala240Val
CA349017813
NM_001371247.1:c.719C>T