Canonical Allele Identifier: PA2573063145
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 439321

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Arg402Lys
CA6403498
NM_000552.5:c.1205G>A