Canonical Allele Identifier: PA2573063578
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100504
ClinVar RCV Id: RCV000086919
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Pro2776Leu
CA228849
NM_000552.5:c.8327C>T