Canonical Allele Identifier: PA2573063403
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100384
ClinVar RCV Id: RCV000086790 RCV002264664
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Gly1573Ser
CA228643
NM_000552.5:c.4717G>A