Canonical Allele Identifier: PA2573063302
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 287
ClinVar RCV Id: RCV000000311 RCV000086709
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Trp1313Cys
CA114121
NM_000552.5:c.3939G>C
CA383506117
NM_000552.5:c.3939G>T