Allele Registry

Canonical Allele Identifier: PA270358

Gene: MECP2 HGNC NCBI

ClinVar RCV:

RCV000133071

ClinVar Variation:

143538

HGVS (amino-acid)	Matching Registered Transcripts
NP_001104262.1:p.Arg123Gly	CA270357 NM_001110792.2:c.367A>G