Canonical Allele Identifier: PA2573063068
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100196
ClinVar RCV Id: RCV000086582 RCV000477864 RCV000851726 RCV003313777
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Ala641Val
CA228298
NM_000552.5:c.1922C>T