Canonical Allele Identifier: PA2741815551
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 2921234
ClinVar RCV Id: RCV003740640

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Cys350Arg
CA383505336
NM_000552.5:c.1048T>C