Canonical Allele Identifier: PA2573063478
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100436
ClinVar RCV Id: RCV000086848 RCV000177861 RCV000400661 RCV002243747 RCV002243749 RCV002243748
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Pro2063Ser
CA202650
NM_000552.5:c.6187C>T