Canonical Allele Identifier: PA2573063400
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 256682
ClinVar RCV Id: RCV000244522 RCV000382042 RCV001812685 RCV002244026 RCV002244027 RCV002244025
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Val1565Leu
CA6402474
NM_000552.5:c.4693G>T
CA383500140
NM_000552.5:c.4693G>C