Canonical Allele Identifier: PA2573063447
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100421
ClinVar RCV Id: RCV000086831 RCV002271338
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Trp1745Cys
CA228706
NM_000552.5:c.5235G>T
CA383496187
NM_000552.5:c.5235G>C