Allele Registry

Canonical Allele Identifier: PA2741904423

Gene: CILP HGNC NCBI

ClinVar RCV:

RCV003982328

ClinVar Variation:

3060299

HGVS (amino-acid)	Matching Registered Transcripts
NP_003604.4:p.Gly1166Ser	CA7615075 NM_003613.4:c.3496G>A