Canonical Allele Identifier: PA2573063381
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 304
ClinVar RCV Id: RCV000000331 RCV000086775
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Phe1514Cys
CA114154
NM_000552.5:c.4541T>G