Canonical Allele Identifier: PA2573063192
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 31011
ClinVar RCV Id: RCV000024003 RCV000086595
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Arg760His
CA228316
NM_000552.5:c.2279G>A