Canonical Allele Identifier: PA232947
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143480

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Glu495Asp
CA232945
NM_001110792.2:c.1485G>C
CA415162879
NM_001110792.2:c.1485G>T