Canonical Allele Identifier: PA2573063273
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 310068
ClinVar RCV Id: RCV000327886 RCV001284371
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Pro1240Leu
CA6402693
NM_000552.5:c.3719C>T