Allele Registry

Canonical Allele Identifier: PA112115

Gene: CTSF HGNC NCBI

ClinVar Allele:

75250

ClinVar RCV:

RCV000054490

ClinVar Variation:

60675

HGVS (amino-acid)	Matching Registered Transcripts
NP_003784.2:p.Gln321Arg	CA144616 NM_003793.4:c.962A>G