Allele Registry

Canonical Allele Identifier: PA2828325160

Gene: MECP2 HGNC NCBI

ClinVar Variation Id: 143606

HGVS (amino-acid)	Matching Registered Transcripts
NP_001356320.1:p.Pro79Ser	CA170310 NM_001369391.2:c.235C>T