Canonical Allele Identifier: PA2573063159
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 439322
ClinVar RCV Id: RCV003993990 RCV003478079 RCV003320360
ClinVar Variation Id: 439323
ClinVar RCV Id: RCV000507666 RCV004023423
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Cys521Ser
CA6403339
NM_000552.5:c.1562G>C
CA383498356
NM_000552.5:c.1561T>A
CA645509534
NM_000552.5:c.1562_1563delinsCT