Canonical Allele Identifier: PA2580305076
Gene: SCN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2435692
ClinVar RCV Id: RCV003136442
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004579.1:p.Ser29Asn
CA6300535
NM_004588.5:c.86G>A