Canonical Allele Identifier: PA199453
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 156636

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Arg478Gln
CA199452
NM_004992.4:c.1433G>A