Canonical Allele Identifier: PA116808
Gene: BSND HGNC NCBI

Linked Data

ClinVar Variation Id: 4384
ClinVar RCV Id: RCV000004634 RCV001057884 RCV001272340
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_476517.1:p.Met1Ile