Canonical Allele Identifier: PA2828326837
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 717385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Thr55Ala
CA415174791
NM_001369393.2:c.163A>G