Canonical Allele Identifier: PA2573063409
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 310
ClinVar RCV Id: RCV000000338 RCV000086795 RCV000622977 RCV000678772 RCV001255177 RCV001843449 RCV002280857 RCV003313770 RCV004547448
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Tyr1584Cys
CA114162
NM_000552.5:c.4751A>G