Canonical Allele Identifier: PA2829695733
Gene: CIT HGNC NCBI

Linked Data

ClinVar Variation Id: 207865
ClinVar RCV Id: RCV000190154
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009105.1:p.Ser1887Tyr
CA204111
NM_007174.3:c.5660C>A