Canonical Allele Identifier: PA2573063275
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 314
ClinVar RCV Id: RCV000000342 RCV000086676 RCV000314989 RCV000853236 RCV002247228 RCV003313771 RCV004547449
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Pro1266Leu
CA114170
NM_000552.5:c.3797C>T