Allele Registry

Canonical Allele Identifier: PA2826592593

Gene: CST8 HGNC NCBI

ClinVar RCV:

RCV004282544

ClinVar Variation:

2511487

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268659.1:p.Ser120Arg	CA9789704 NM_001281730.2:c.358A>C CA9789705 NM_001281730.2:c.360C>G CA408422435 NM_001281730.2:c.360C>A