Canonical Allele Identifier: PA2573063416
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 286
ClinVar RCV Id: RCV000000310 RCV000086803 RCV002243604
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Val1607Asp
CA114119
NM_000552.5:c.4820T>A