Canonical Allele Identifier: PA2573063297
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100302
ClinVar RCV Id: RCV000086702 RCV002264654
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Leu1307Pro
CA228486
NM_000552.5:c.3920T>C