Allele Registry

Canonical Allele Identifier: PA2826955987

Gene: MECP2 HGNC NCBI

ClinVar Variation Id: 143756

HGVS (amino-acid)	Matching Registered Transcripts
NP_001303266.1:p.Leu235Val	CA270593 NM_001316337.2:c.703C>G