Canonical Allele Identifier: PA2573063581
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100505
ClinVar RCV Id: RCV000086920
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Pro2781Ser
CA228851
NM_000552.5:c.8341C>T