Allele Registry

Canonical Allele Identifier: PA2499291284

Gene: CEP135 HGNC NCBI

ClinVar RCV:

RCV001334251

ClinVar Variation:

1032208

HGVS (amino-acid)	Matching Registered Transcripts
NP_079285.2:p.Arg77Ser	CA356965255 NM_025009.5:c.231A>C CA356965257 NM_025009.5:c.231A>T