Canonical Allele Identifier: PA2825358428
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 464902
ClinVar RCV Id: RCV000713068 RCV001078766
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035233.1:p.Arg524Gln
CA1939839
NM_001040143.2:c.1571G>A