Canonical Allele Identifier: PA317967
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 207000
ClinVar RCV Id: RCV000189151
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Arg1435Gly
CA317965
NM_021007.3:c.4303C>G