Canonical Allele Identifier: PA2573063332
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100327
ClinVar RCV Id: RCV000086732 RCV000678769 RCV002243736 RCV003226195
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Ile1372Ser
CA228535
NM_000552.5:c.4115T>G