Canonical Allele Identifier: PA2573063417
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100395
ClinVar RCV Id: RCV000086804 RCV002243743 RCV003387760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Gly1609Arg
CA228665
NM_000552.5:c.4825G>A
CA383499042
NM_000552.5:c.4825G>C