Canonical Allele Identifier: PA211307
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 95187

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Glu397Lys
CA211306
NM_004992.4:c.1189G>A