Canonical Allele Identifier: PA2580406873
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_057368.3:p.Ile1715Thr
CA396166246
NM_016284.5:c.5144T>C