Canonical Allele Identifier: PA645455562
Gene: CNOT9 HGNC NCBI

Linked Data

ClinVar Variation Id: 376527
ClinVar RCV Id: RCV000426322 RCV000427048 RCV000434591 RCV000443624 RCV000444398
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005435.1:p.Ser87Cys
CA16602956
NM_005444.3:c.260C>G