Canonical Allele Identifier: PA2573063423
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 284
ClinVar RCV Id: RCV000000308 RCV000086808 RCV000778377 RCV002243602
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Ile1628Thr
CA114115
NM_000552.5:c.4883T>C