Canonical Allele Identifier: PA2573063320
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100317
ClinVar RCV Id: RCV000086722 RCV002264656
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Arg1341Pro
CA228516
NM_000552.5:c.4022G>C