Canonical Allele Identifier: PA2573063161
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 318
ClinVar RCV Id: RCV000000346 RCV000086569 RCV002243608
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Asn528Ser
CA114178
NM_000552.5:c.1583A>G