Canonical Allele Identifier: PA2573063252
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100261
ClinVar RCV Id: RCV000086654 RCV002243723
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Cys1130Phe
CA228404
NM_000552.5:c.3389G>T