Canonical Allele Identifier: PA2573063168
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 305
ClinVar RCV Id: RCV000000332 RCV000086570
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Gly550Arg
CA114156
NM_000552.5:c.1648G>A
CA383498180
NM_000552.5:c.1648G>C