Canonical Allele Identifier: PA2573063305
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100308
ClinVar RCV Id: RCV000086710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Val1314Phe
CA228498
NM_000552.5:c.3940G>T