Canonical Allele Identifier: PA2573063064
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 381621
ClinVar RCV Id: RCV000760113 RCV000765104 RCV000852047 RCV003147455 RCV002264696 RCV003323534 RCV004551444
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Ala542Gly
CA6403319
NM_000552.5:c.1625C>G