Canonical Allele Identifier: PA199314
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 138187

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Thr209Met
CA199312
NM_001110792.2:c.626C>T