Canonical Allele Identifier: PA2829476709
Gene: CCN6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1704535
ClinVar RCV Id: RCV002282862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003871.1:p.Gln338Leu
CA3964141
NM_003880.4:c.1013A>T