Canonical Allele Identifier: PA2573063160
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100184
ClinVar RCV Id: RCV000086568
ClinVar Variation Id: 2634000
ClinVar RCV Id: RCV004552507
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Gly525Arg
CA228277
NM_000552.5:c.1573G>A
CA383498333
NM_000552.5:c.1573G>C