Canonical Allele Identifier: PA2825559238
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 717385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Thr160Ala
CA415174791
NM_001110792.2:c.478A>G