Canonical Allele Identifier: PA645486702
Gene: VWA3B HGNC NCBI

Linked Data

ClinVar Variation Id: 226428
ClinVar RCV Id: RCV000211708
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659429.4:p.Lys622Thr
CA10576347
NM_144992.5:c.1865A>C