Canonical Allele Identifier: PA2828506364
Gene: GLI2 HGNC NCBI

Linked Data

ClinVar Variation Id: 235079
ClinVar RCV Id: RCV000223717

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361283.1:p.Thr1444_Ter1445insTyrArgProGluArgLeuValLeuSerAlaProGlyGlyValIleAlaAlaGlnSerLeuGlyIleProAlaValLeuSerPheSerLysLysValLeuAsnArgLeuGluGlyLeuLeuArgAsnGlyArgPheArg
CA10581212
NM_001374354.1:c.4335G>C
CA348180552
NM_001374354.1:c.4335G>T