Canonical Allele Identifier: PA099529
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 11811

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Thr158Met
CA211252
NM_004992.4:c.473C>T