ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2573063413
Gene: VWF
HGNC
NCBI
Linked Data
ClinVar Variation Id:
285
ClinVar RCV Id:
RCV000000309
RCV000086797
RCV000623564
RCV000999877
RCV000851942
RCV002243603
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000543.3:p.Arg1597Trp
CA114117
NM_000552.5:c.4789C>T