Canonical Allele Identifier: PA2573063231
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100243
ClinVar RCV Id: RCV000086635 RCV002264642
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Ser979Asn
CA228372
NM_000552.5:c.2936G>A