Canonical Allele Identifier: PA2573063257
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 309
ClinVar RCV Id: RCV000000337 RCV000086657 RCV002264636
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Cys1149Arg
CA228410
NM_000552.5:c.3445T>C