Allele Registry

Canonical Allele Identifier: PA112125

Gene: CTSF HGNC NCBI

ClinVar RCV:

RCV000054491

ClinVar Variation:

60676

HGVS (amino-acid)	Matching Registered Transcripts
NP_003784.2:p.Gly458Ala	CA144617 NM_003793.4:c.1373G>C