Canonical Allele Identifier: PA2573063129
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100496
ClinVar RCV Id: RCV000086910 RCV001787084
ClinVar Variation Id: 1698609
ClinVar RCV Id: RCV002271886
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Cys275Ser
CA228834
NM_000552.5:c.823T>A
CA383508439
NM_000552.5:c.824G>C