Canonical Allele Identifier: PA2829476706
Gene: CCN6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1680476
ClinVar RCV Id: RCV002236536
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003871.1:p.Ser334Thr
CA365376698
NM_003880.4:c.1000T>A