Canonical Allele Identifier: PA2829695711
Gene: CIT HGNC NCBI

Linked Data

ClinVar Variation Id: 592099
ClinVar RCV Id: RCV000723290 RCV002533073
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009105.1:p.Thr1760Met
CA6820903
NM_007174.3:c.5279C>T