Canonical Allele Identifier: PA645455010
Gene: SCN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 408875
ClinVar RCV Id: RCV000464872 RCV002393126
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004579.1:p.Arg47His
CA6300517
NM_004588.5:c.140G>A