Canonical Allele Identifier: PA2573063074
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 439332
ClinVar RCV Id: RCV000851647 RCV002274046
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Arg1205Cys
CA6402724
NM_000552.5:c.3613C>T