Canonical Allele Identifier: PA2573063220
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 296
ClinVar RCV Id: RCV000000320 RCV000000321 RCV000086620 RCV000169683 RCV000336497 RCV000762901 RCV000851593 RCV001270529 RCV004547445 RCV003987302
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Arg854Gln
CA114139
NM_000552.5:c.2561G>A