Canonical Allele Identifier: PA2573063116
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100338
ClinVar RCV Id: RCV000086743 RCV000852120 RCV002264661
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Asp141Asn
CA228557
NM_000552.5:c.421G>A