Canonical Allele Identifier: PA302150
Gene: SCN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 190857
ClinVar RCV Id: RCV000171036 RCV000765438 RCV000559019 RCV002381546
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001028.1:p.Arg45His
CA302149
NM_001037.5:c.134G>A