Canonical Allele Identifier: PA645415766
Gene: SCN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 436652
ClinVar RCV Id: RCV000503065 RCV000815939 RCV001764493 RCV002476008
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001028.1:p.Arg45Cys
CA9371961
NM_001037.5:c.133C>T