Canonical Allele Identifier: PA2573063504
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100450
ClinVar RCV Id: RCV000086862 RCV000765102 RCV002265605 RCV003387761
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Arg2287Trp
CA228760
NM_000552.5:c.6859C>T