Canonical Allele Identifier: PA204112
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_001193928.1:p.Ser1929Tyr
CA204111
NM_001206999.1:c.5786C>A