Canonical Allele Identifier: PA2573063210
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 312
ClinVar RCV Id: RCV000000340 RCV000086607
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Tyr795Cys
CA114166
NM_000552.5:c.2384A>G