Canonical Allele Identifier: PA2573063438
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100412
ClinVar RCV Id: RCV000086822 RCV002243744
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Val1665Glu
CA228692
NM_000552.5:c.4994T>A