Canonical Allele Identifier: PA2580174938
Gene: CIT HGNC NCBI

Linked Data

ClinVar Variation Id: 2033914
ClinVar RCV Id: RCV002872735
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193928.1:p.Leu2057Pro
CA6820629
NM_001206999.1:c.6170T>C