Canonical Allele Identifier: PA2573063100
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100432
ClinVar RCV Id: RCV000086844 RCV002264667 RCV003478999
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Gly19Arg
CA228729
NM_000552.5:c.55G>A
CA383510446
NM_000552.5:c.55G>C