Canonical Allele Identifier: PA2573063574
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100500
ClinVar RCV Id: RCV000086914
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Cys2771Ser
CA228842
NM_000552.5:c.8311T>A
CA383486669
NM_000552.5:c.8312G>C