Canonical Allele Identifier: PA2826488055
Gene: CNOT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2100051
ClinVar RCV Id: RCV003025788
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001252541.1:p.Ile1710Thr
CA396166246
NM_001265612.2:c.5129T>C