Canonical Allele Identifier: PA2573063171
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100188
ClinVar RCV Id: RCV000086574 RCV000343818 RCV000506040
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Met576Ile
CA228284
NM_000552.5:c.1728G>T
CA383497810
NM_000552.5:c.1728G>C
CA383497811
NM_000552.5:c.1728G>A