Canonical Allele Identifier: PA1139765297
Gene: CCN6 HGNC NCBI

Linked Data

ClinVar Variation Id: 355061

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937882.2:p.Arg60Cys
CA3963925
NM_198239.2:c.178C>T