Canonical Allele Identifier: PA2573063511
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 310044
ClinVar RCV Id: RCV000361746
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Pro2336Leu
CA6401803
NM_000552.5:c.7007C>T