Canonical Allele Identifier: PA2573063528
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100467
ClinVar RCV Id: RCV000086880 RCV000778374 RCV001270490 RCV002264670
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Arg2464Cys
CA228786
NM_000552.5:c.7390C>T