Canonical Allele Identifier: PA2573063128
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100493
ClinVar RCV Id: RCV000086907 RCV003398701 RCV003313936
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Arg273Trp
CA228829
NM_000552.5:c.817C>T