Canonical Allele Identifier: PA2828474066
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 943227
ClinVar RCV Id: RCV002285456 RCV001213373
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Asp301Asn
CA349018557
NM_001371247.1:c.901G>A