Canonical Allele Identifier: PA2826056479
Gene: CITED2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1174691
ClinVar RCV Id: RCV001528478

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161860.1:p.Ser181Thr
CA4025588
NM_001168388.2:c.542G>C