Canonical Allele Identifier: PA2573063319
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 291
ClinVar RCV Id: RCV000000315 RCV000086721 RCV002227435 RCV002243605 RCV004547443
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Arg1341Gln
CA114129
NM_000552.5:c.4022G>A