Canonical Allele Identifier: PA1139765372
Gene: CCN6 HGNC NCBI

Linked Data

ClinVar Variation Id: 6388

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937882.2:p.Ser334Pro
CA118183
NM_198239.2:c.1000T>C