Canonical Allele Identifier: PA2825192269
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 3189440
ClinVar RCV Id: RCV004485318
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Asp1087Asn
CA6402787
NM_000552.5:c.3259G>A