Canonical Allele Identifier: PA2573063561
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100489
ClinVar RCV Id: RCV000086903

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Cys2693Tyr
CA228823
NM_000552.5:c.8078G>A