Canonical Allele Identifier: PA2827354747
Gene: VWA3B HGNC NCBI

Linked Data

ClinVar Variation Id: 226428
ClinVar RCV Id: RCV000211708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001332793.1:p.Lys279Thr
CA10576347
NM_001345864.2:c.836A>C