Canonical Allele Identifier: PA072943
Gene: ZNF687 HGNC NCBI

Linked Data

ClinVar Variation Id: 222987
ClinVar RCV Id: RCV000208586 RCV002515559
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291693.1:p.Pro937Arg
CA072935
NM_001304764.2:c.2810C>G