Canonical Allele Identifier: PA2580118954
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 2429680
ClinVar RCV Id: RCV003127134

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Ala1773Thr
CA383495764
NM_000552.5:c.5317G>A