Canonical Allele Identifier: PA2573063256
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 31009
ClinVar RCV Id: RCV000024001 RCV000086656 RCV000851956 RCV001800314 RCV002264640
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Tyr1146Cys
CA228408
NM_000552.5:c.3437A>G