Canonical Allele Identifier: PA2573063516
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 315
ClinVar RCV Id: RCV000000343 RCV000086870
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Cys2362Phe
CA114172
NM_000552.5:c.7085G>T