Canonical Allele Identifier: PA259905
Gene: CENPJ HGNC NCBI

Linked Data

ClinVar Variation Id: 30783

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060921.3:p.Thr821Met
CA259904
NM_018451.5:c.2462C>T