Canonical Allele Identifier: PA2826529512
Gene: CNOT9 HGNC NCBI

Linked Data

ClinVar Variation Id: 376527
ClinVar RCV Id: RCV000426322 RCV000427048 RCV000434591 RCV000443624 RCV000444398
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258564.1:p.Ser87Cys
CA16602956
NM_001271635.1:c.260C>G