Canonical Allele Identifier: PA2573063445
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100420
ClinVar RCV Id: RCV000086830 RCV000343743 RCV000826083 RCV004549531 RCV002243746
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Ser1731Thr
CA228704
NM_000552.5:c.5191T>A