Canonical Allele Identifier: PA2573063325
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100321
ClinVar RCV Id: RCV000086726 RCV002264657
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Glu1359Lys
CA228524
NM_000552.5:c.4075G>A