Canonical Allele Identifier: PA2573063493
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100442
ClinVar RCV Id: RCV000086854 RCV002264668
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Ser2179Phe
CA228746
NM_000552.5:c.6536C>T