Canonical Allele Identifier: PA658812006
Gene: CCN6 HGNC NCBI

Linked Data

ClinVar Variation Id: 521955

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003871.1:p.Cys337Tyr
CA365376780
NM_003880.4:c.1010G>A