Canonical Allele Identifier: PA2573063575
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100501
ClinVar RCV Id: RCV000086915

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Cys2771Tyr
CA228844
NM_000552.5:c.8312G>A