Canonical Allele Identifier: PA2573063164
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 627250
ClinVar RCV Id: RCV000852041 RCV002264736
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Leu536Pro
CA383498252
NM_000552.5:c.1607T>C