Allele Registry

Canonical Allele Identifier: PA170356

Gene: MECP2 HGNC NCBI

ClinVar RCV:

RCV000133197

RCV001522685

RCV002472328

ClinVar Variation:

143656

HGVS (amino-acid)	Matching Registered Transcripts
NP_004983.1:p.Gln227Glu	CA170355 NM_004992.4:c.679C>G