Canonical Allele Identifier: PA2573063584
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 437264
ClinVar RCV Id: RCV000500840 RCV000756906 RCV004551638
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Val2793Ala
CA6401320
NM_000552.5:c.8378T>C