Canonical Allele Identifier: PA645455013
Gene: SCN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 408876
ClinVar RCV Id: RCV000472431 RCV002436428
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004579.1:p.Arg84Cys
CA6300493
NM_004588.5:c.250C>T