Canonical Allele Identifier: PA274539
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143559

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Arg145His
CA274538
NM_001110792.2:c.434G>A