Canonical Allele Identifier: PA2573063443
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 619937
ClinVar RCV Id: RCV000760125
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Pro1725Ser
CA6402355
NM_000552.5:c.5173C>T