Canonical Allele Identifier: PA2826240700
Gene: CNOT2 HGNC NCBI
ClinVar RCV:
RCV002652699
ClinVar Variation:
2209448
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186231.1:p.Pro107Leu
CA239426678
NM_001199302.2:c.320C>T