Canonical Allele Identifier: PA2573063457
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100427
ClinVar RCV Id: RCV000086838 RCV002264666
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Lys1794Glu
CA228719
NM_000552.5:c.5380A>G