Canonical Allele Identifier: PA270413
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143569

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Tyr153Cys
CA270411
NM_001110792.2:c.458A>G