Canonical Allele Identifier: PA256090
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 11814

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Arg118Trp
CA256089
NM_001110792.2:c.352C>T