Canonical Allele Identifier: PA112115
Gene: CTSF HGNC NCBI

Linked Data

ClinVar Variation Id: 60675
ClinVar RCV Id: RCV000054490
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Amino-acid Alleles

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