Canonical Allele Identifier: PA2573063555
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 372760
ClinVar RCV Id: RCV000413262 RCV000851890 RCV000986090 RCV000778372 RCV001270575 RCV002280878
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Arg2663Pro
CA6401423
NM_000552.5:c.7988G>C