Canonical Allele Identifier: PA2573063263
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100268
ClinVar RCV Id: RCV000086663 RCV001093531 RCV003126497
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Gly1180Arg
CA228421
NM_000552.5:c.3538G>A
CA383511143
NM_000552.5:c.3538G>C