Canonical Allele Identifier: PA2573063190
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100206
ClinVar RCV Id: RCV000086592 RCV000175146 RCV000267455 RCV002243713 RCV002243714 RCV002243715
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Met740Ile
CA201316
NM_000552.5:c.2220G>A
CA383523428
NM_000552.5:c.2220G>C
CA383523429
NM_000552.5:c.2220G>T