Canonical Allele Identifier: PA2741815696
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 2664688
ClinVar RCV Id: RCV003447663

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Val1083Ile
CA383512303
NM_000552.5:c.3247G>A