Canonical Allele Identifier: PA2573063304
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 302
ClinVar RCV Id: RCV000000329 RCV000087017
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Val1314Leu
CA114151
NM_000552.5:c.3940G>C