Canonical Allele Identifier: PA2573063212
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 313
ClinVar RCV Id: RCV000000341 RCV000086609
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Cys804Phe
CA114168
NM_000552.5:c.2411G>T