Canonical Allele Identifier: PA2573063270
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100274
ClinVar RCV Id: RCV000086670 RCV000250437 RCV000851979 RCV002243724 RCV002264649 RCV002264647 RCV002264648
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Val1229Gly
CA228433
NM_000552.5:c.3686T>G