Canonical Allele Identifier: PA2573063172
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 391499
ClinVar RCV Id: RCV000759383 RCV001821208 RCV004551498 RCV002506077
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Arg606Gln
CA6403256
NM_000552.5:c.1817G>A