Canonical Allele Identifier: PA2741974338
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2945553
ClinVar RCV Id: RCV003803647
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Tyr1092His
CA349021646
NM_021007.3:c.3274T>C