Canonical Allele Identifier: PA2829695764
Gene: CIT HGNC NCBI

Linked Data

ClinVar Variation Id: 2033914
ClinVar RCV Id: RCV002872735
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009105.1:p.Leu2015Pro
CA6820629
NM_007174.3:c.6044T>C