Canonical Allele Identifier: PA2573063221
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 417966
ClinVar RCV Id: RCV000477961 RCV000852094
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Asn857Ser
CA6403020
NM_000552.5:c.2570A>G