Allele Registry

Canonical Allele Identifier: PA2499264322

Gene: CILP HGNC NCBI

ClinVar RCV:

RCV001355618

ClinVar Variation:

1049471

HGVS (amino-acid)	Matching Registered Transcripts
NP_003604.4:p.Val1113Ala	CA271504437 NM_003613.4:c.3338T>C