Canonical Allele Identifier: PA096192
Gene: SCN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 60769
ClinVar RCV Id: RCV000054539 RCV000483016 RCV002426610
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004579.1:p.Arg28Trp
CA214436
NM_004588.5:c.82C>T