Canonical Allele Identifier: PA2573063271
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100275
ClinVar RCV Id: RCV000086671 RCV000242240 RCV000851980 RCV002243725
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Asn1231Thr
CA228435
NM_000552.5:c.3692A>C