Allele Registry

Canonical Allele Identifier: PA072939

Gene: ZNF687 HGNC NCBI

ClinVar RCV:

RCV000208586

RCV002515559

ClinVar Variation:

222987

HGVS (amino-acid)	Matching Registered Transcripts
NP_001291692.1:p.Pro937Arg	CA072935 NM_001304763.2:c.2810C>G