Canonical Allele Identifier: PA118184
Gene: CCN6 HGNC NCBI

Linked Data

ClinVar Variation Id: 6388

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003871.1:p.Ser334Pro
CA118183
NM_003880.4:c.1000T>C