Allele Registry

Canonical Allele Identifier: PA121706

Gene: MECP2 HGNC NCBI

ClinVar RCV:

RCV000012598

RCV001230698

RCV001566839

ClinVar Variation:

11825

HGVS (amino-acid)	Matching Registered Transcripts
NP_001104262.1:p.Glu149Gly	CA121705 NM_001110792.2:c.446A>G