Canonical Allele Identifier: PA2829753054
Gene: CNOT2 HGNC NCBI
ClinVar RCV:
RCV002652699
ClinVar Variation:
2209448
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055330.1:p.Pro107Leu
CA239426678
NM_014515.7:c.320C>T