Canonical Allele Identifier: PA1139755592
Gene: BSND HGNC NCBI

Linked Data

ClinVar Variation Id: 992426
ClinVar RCV Id: RCV001280872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_476517.1:p.Gly22Arg
CA871203
NM_057176.3:c.64G>C