Canonical Allele Identifier: PA2573063098
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100506
ClinVar RCV Id: RCV000086921
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Ala2801Asp
CA228853
NM_000552.5:c.8402C>A