Canonical Allele Identifier: PA2580118466
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 1802692
ClinVar RCV Id: RCV002465970

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Ala1098Thr
CA6402781
NM_000552.5:c.3292G>A