Allele Registry

Canonical Allele Identifier: PA121714

Gene: MECP2 HGNC NCBI

ClinVar RCV:

RCV000012615

RCV000133194

ClinVar Variation:

11841

HGVS (amino-acid)	Matching Registered Transcripts
NP_001104262.1:p.Pro237Leu	CA121713 NM_001110792.2:c.710C>T