Canonical Allele Identifier: PA2826955564
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3124838
ClinVar RCV Id: RCV004421695

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Asp28His
CA415176516
NM_001316337.2:c.82G>C