Canonical Allele Identifier: PA2573063086
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100347
ClinVar RCV Id: RCV000086752 RCV002243741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Ala1437Thr
CA228575
NM_000552.5:c.4309G>A