Allele Registry

Canonical Allele Identifier: PA2828325871

Gene: MECP2 HGNC NCBI

ClinVar RCV:

RCV000133059

ClinVar Variation:

143527

HGVS (amino-acid)	Matching Registered Transcripts
NP_001356321.1:p.Pro8Leu	CA270332 NM_001369392.2:c.23C>T