Canonical Allele Identifier: PA1139726037
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 940493
ClinVar RCV Id: RCV001210090
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Phe1590Ser
CA1940317
NM_021007.3:c.4769T>C