Canonical Allele Identifier: PA2499233456
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100299
ClinVar RCV Id: RCV000086698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Met1304dup
CA228480
NM_000552.5:c.3910_3912dup