Canonical Allele Identifier: PA2573063166
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 801294
ClinVar RCV Id: RCV000986060 RCV003479258
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Pro538Leu
CA6403326
NM_000552.5:c.1613C>T