Canonical Allele Identifier: PA2573063548
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100480
ClinVar RCV Id: RCV000086894 RCV001787076 RCV002225289
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Asn2546Tyr
CA228810
NM_000552.5:c.7636A>T