Canonical Allele Identifier: PA2573063396
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100380
ClinVar RCV Id: RCV000086786 RCV002264663
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Gln1556Arg
CA228635
NM_000552.5:c.4667A>G