Allele Registry

Canonical Allele Identifier: PA2828326741

Gene: MECP2 HGNC NCBI

ClinVar Variation Id: 143526

HGVS (amino-acid)	Matching Registered Transcripts
NP_001356322.1:p.Pro8Arg	CA274626 NM_001369393.2:c.23C>G