Canonical Allele Identifier: PA2573063557
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 235639
ClinVar RCV Id: RCV000224741 RCV000323842 RCV002243901 RCV002243902 RCV002243903 RCV004547572
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Thr2666Met
CA6401422
NM_000552.5:c.7997C>T