Allele Registry

Canonical Allele Identifier: PA1139765374

Gene: CCN6 HGNC NCBI

ClinVar Variation Id: 521955

HGVS (amino-acid)	Matching Registered Transcripts
NP_937882.2:p.Cys337Tyr	CA365376780 NM_198239.2:c.1010G>A