Canonical Allele Identifier: PA2573063237
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100248
ClinVar RCV Id: RCV000086641 RCV002264643 RCV002264644
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Cys1060Tyr
CA228380
NM_000552.5:c.3179G>A