Canonical Allele Identifier: PA1139765288
Gene: CCN6 HGNC NCBI

Linked Data

ClinVar Variation Id: 355059

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937882.2:p.Pro31Thr
CA3963911
NM_198239.2:c.91C>A