Canonical Allele Identifier: PA2573063554
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100487
ClinVar RCV Id: RCV000086901 RCV000765101 RCV000851886 RCV002225290 RCV002225291
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Thr2647Met
CA228819
NM_000552.5:c.7940C>T