Canonical Allele Identifier: PA1139741979
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 948341
ClinVar RCV Id: RCV001219575
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Lys120Ile
CA349011856
NM_021007.3:c.359A>T