Canonical Allele Identifier: PA205185
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 211466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Arg262Cys
CA205183
NM_001110792.2:c.784C>T