Canonical Allele Identifier: PA645498092
Gene: CCN6 HGNC NCBI

Linked Data

ClinVar Variation Id: 355059

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003871.1:p.Pro31Thr
CA3963911
NM_003880.4:c.91C>A