Canonical Allele Identifier: PA094614
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 12878
ClinVar RCV Id: RCV000013738 RCV000189121 RCV000527590 RCV003224096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Val892Ile
CA122770
NM_001040142.2:c.2674G>A