Canonical Allele Identifier: PA2573063270
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100274

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Val1229Gly
CA228433
NM_000552.5:c.3686T>G