Allele Registry

Canonical Allele Identifier: PA118177

Gene: CCN6 HGNC NCBI

ClinVar Allele:

21418

ClinVar RCV:

RCV000006751

ClinVar Variation:

6379

HGVS (amino-acid)	Matching Registered Transcripts
NP_003871.1:p.Cys145Tyr	CA118176 NM_003880.4:c.434G>A