Canonical Allele Identifier: PA2573063264
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100269
ClinVar RCV Id: RCV000086664 RCV000851643 RCV001787054 RCV002264646
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Cys1190Arg
CA228423
NM_000552.5:c.3568T>C