Canonical Allele Identifier: PA116813
Gene: BSND HGNC NCBI

Linked Data

ClinVar Variation Id: 4388
ClinVar RCV Id: RCV000004638 RCV000785598 RCV001214565 RCV002281695 RCV001291206
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_476517.1:p.Ile12Thr
CA116812
NM_057176.3:c.35T>C