Canonical Allele Identifier: PA2573063451
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100423
ClinVar RCV Id: RCV000086833 RCV000852152
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Leu1774Ser
CA228710
NM_000552.5:c.5321T>C