Canonical Allele Identifier: PA645400574
Gene: CTSF HGNC NCBI

Linked Data

ClinVar Variation Id: 424983
ClinVar RCV Id: RCV000487825 RCV001085523 RCV002318587 RCV003932784
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003784.2:p.Thr228Arg
CA6125485
NM_003793.4:c.683C>G