Canonical Allele Identifier: PA658811999
Gene: CCN6 HGNC NCBI

Linked Data

ClinVar Variation Id: 500275
ClinVar RCV Id: RCV000592704 RCV001510300 RCV003615849 RCV003900332
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003871.1:p.Asn178Ile
CA3964006
NM_003880.4:c.533A>T