Canonical Allele Identifier: PA2573063084
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100312
ClinVar RCV Id: RCV000086714 RCV002243733
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Arg1315Leu
CA228506
NM_000552.5:c.3944G>T