Canonical Allele Identifier: PA232910
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Pro403del
CA1138553958
NM_001110792.2:c.1200_1202del
CA2695100356
NM_001110792.2:c.1206_1208del
CA2695100362
NM_001110792.2:c.1203_1205del