Canonical Allele Identifier: PA645400579
Gene: CTSF HGNC NCBI

Linked Data

ClinVar Variation Id: 285170
ClinVar RCV Id: RCV000372587 RCV002321956
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003784.2:p.Asn378Ser
CA6125312
NM_003793.4:c.1133A>G