Canonical Allele Identifier: PA2580118219
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 1695364
ClinVar RCV Id: RCV002264867
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Asp534Asn
CA383498271
NM_000552.5:c.1600G>A