Canonical Allele Identifier: PA891866031
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_001193928.1:p.Thr1802Met
CA6820903
NM_001206999.1:c.5405C>T