Canonical Allele Identifier: PA2573063334
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100330
ClinVar RCV Id: RCV000086735 RCV000626712 RCV001093529 RCV000851939 RCV000852116 RCV002264658
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Arg1374His
CA228541
NM_000552.5:c.4121G>A