Canonical Allele Identifier: PA2573063327
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100323
ClinVar RCV Id: RCV000086728 RCV000678768 RCV000851781
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Leu1361Ser
CA228528
NM_000552.5:c.4082T>C