Canonical Allele Identifier: PA2573063274
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100279
ClinVar RCV Id: RCV000086675 RCV000678765 RCV001823113 RCV002247493 RCV002281924 RCV002490753 RCV004549528
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Pro1266Gln
CA228441
NM_000552.5:c.3797C>A