Allele Registry

Canonical Allele Identifier: PA202771

Gene: MECP2 HGNC NCBI

ClinVar RCV:

RCV000081204

RCV000169946

RCV000445574

RCV000815972

ClinVar Variation:

95196

393489

HGVS (amino-acid)	Matching Registered Transcripts
NP_001104262.1:p.Asp168Glu	CA202769 NM_001110792.2:c.504C>G CA16609353 NM_001110792.2:c.504C>A