Canonical Allele Identifier: PA645392686
Gene: CEACAM16 HGNC NCBI

Linked Data

ClinVar Variation Id: 281644

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001034302.2:p.Thr290Met
CA9503163
NM_001039213.4:c.869C>T