Canonical Allele Identifier: PA645498106
Gene: CCN6 HGNC NCBI

Linked Data

ClinVar Variation Id: 355061

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003871.1:p.Arg60Cys
CA3963925
NM_003880.4:c.178C>T