Canonical Allele Identifier: PA2573063306
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 290
ClinVar RCV Id: RCV000000314 RCV000086715 RCV000507168 RCV000678767 RCV000851771 RCV002476901
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Val1316Met
CA114127
NM_000552.5:c.3946G>A