Canonical Allele Identifier: PA2825844444
Gene: SCN4B HGNC NCBI

Linked Data

ClinVar Variation Id: 1744112
ClinVar RCV Id: RCV002340715
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135820.1:p.Leu30His
CA382777609
NM_001142348.2:c.89T>A