Canonical Allele Identifier: PA2573063418
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 292
ClinVar RCV Id: RCV000000316 RCV000086805
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Ser1613Pro
CA114131
NM_000552.5:c.4837T>C