Canonical Allele Identifier: PA2826529501
Gene: CNOT9 HGNC NCBI

Linked Data

ClinVar Variation Id: 376526
ClinVar RCV Id: RCV000421602 RCV000422236 RCV000431636 RCV000431838 RCV000438382
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258563.1:p.Ser87Pro
CA16602955
NM_001271634.1:c.259T>C