Canonical Allele Identifier: PA2826529505
Gene: CNOT9 HGNC NCBI

Linked Data

ClinVar Variation Id: 376525
ClinVar RCV Id: RCV000439915

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258563.1:p.Pro131Ser
CA16602954
NM_001271634.1:c.391C>T