Canonical Allele Identifier: PA2573063276
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100280
ClinVar RCV Id: RCV000086677
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.His1268Asn
CA228443
NM_000552.5:c.3802C>A