Canonical Allele Identifier: PA233018
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143747

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Arg318Leu
CA233016
NM_001110792.2:c.953G>T