Canonical Allele Identifier: PA2573063456
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 196665
ClinVar RCV Id: RCV000177518 RCV000330483
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Pro1790Leu
CA243723
NM_000552.5:c.5369C>T