Allele Registry

Canonical Allele Identifier: PA112436

Gene: CCN6 HGNC NCBI

ClinVar RCV:

RCV000006754

ClinVar Variation:

6382

HGVS (amino-acid)	Matching Registered Transcripts
NP_003871.1:p.Cys78Arg	CA118182 NM_003880.4:c.232T>C