Canonical Allele Identifier: PA2573063366
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100355
ClinVar RCV Id: RCV000086760 RCV002466430
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Pro1462Ala
CA228590
NM_000552.5:c.4384C>G