Canonical Allele Identifier: PA2580174925
Gene: CIT HGNC NCBI
ClinVar RCV:
RCV002824189
ClinVar Variation:
1997805
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193928.1:p.Arg1861Cys
CA6820815
NM_001206999.1:c.5581C>T