Canonical Allele Identifier: PA2573063236
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100247
ClinVar RCV Id: RCV000086639 RCV003447495
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Gln1053His
CA228378
NM_000552.5:c.3159G>T
CA383513660
NM_000552.5:c.3159G>C