Canonical Allele Identifier: PA2573063293
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100295
ClinVar RCV Id: RCV000086694 RCV002264653
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Phe1293Leu
CA228472
NM_000552.5:c.3877T>C
CA383506537
NM_000552.5:c.3879T>G
CA383506541
NM_000552.5:c.3879T>A