Canonical Allele Identifier: PA915991351
Gene: CILP HGNC NCBI

Linked Data

ClinVar Variation Id: 6312

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003604.4:p.Ile395Thr
CA118128
NM_003613.4:c.1184T>C