Allele Registry

Canonical Allele Identifier: PA2741904414

Gene: CILP HGNC NCBI

ClinVar RCV:

RCV003979533

ClinVar Variation:

3058903

HGVS (amino-acid)	Matching Registered Transcripts
NP_003604.4:p.Gln979Arg	CA7615202 NM_003613.4:c.2936A>G