Canonical Allele Identifier: PA2573063209
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 294
ClinVar RCV Id: RCV000000318 RCV000086606 RCV000851745 RCV002227436 RCV002264633
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Thr791Met
CA114135
NM_000552.5:c.2372C>T