Canonical Allele Identifier: PA118177
Gene: CCN6 HGNC NCBI

Linked Data

ClinVar Variation Id: 6379
ClinVar RCV Id: RCV000006751
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003871.1:p.Cys145Tyr
CA118176
NM_003880.4:c.434G>A