Allele Registry

Canonical Allele Identifier: PA121709

Gene: MECP2 HGNC NCBI

ClinVar RCV:

RCV000012604

RCV000132982

RCV001719695

RCV002260597

RCV002371770

RCV004540997

ClinVar Variation:

11831

HGVS (amino-acid)	Matching Registered Transcripts
NP_001104262.1:p.Gly440Ser	CA121707 NM_001110792.2:c.1318G>A