Canonical Allele Identifier: PA2573063289
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100292
ClinVar RCV Id: RCV000086690 RCV002264650
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Ser1285Pro
CA228466
NM_000552.5:c.3853T>C