Canonical Allele Identifier: PA915990522
Gene: CITED2 HGNC NCBI

Linked Data

ClinVar Variation Id: 668342
ClinVar RCV Id: RCV000827195
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161861.2:p.Ser197Gly
CA4025578
NM_001168389.2:c.589A>G