Canonical Allele Identifier: PA2573063191
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100208
ClinVar RCV Id: RCV000086594 RCV003147338 RCV003992184
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Arg760Cys
CA228314
NM_000552.5:c.2278C>T