Canonical Allele Identifier: PA2828470739
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1342678
ClinVar RCV Id: RCV001847351
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358175.1:p.Leu377del
CA2573051692
NM_001371246.1:c.1128_1130del