Canonical Allele Identifier: PA2825559203
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2445701
ClinVar RCV Id: RCV003155620

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Ala129Gly
CA415176615
NM_001110792.2:c.386C>G