Canonical Allele Identifier: PA2741974558
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2943871
ClinVar RCV Id: RCV003803429 RCV003989864
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Ile1541Met
CA349036308
NM_021007.3:c.4623C>G