Canonical Allele Identifier: PA2573063296
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100298
ClinVar RCV Id: RCV000086697

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Met1304Val
CA228478
NM_000552.5:c.3910A>G