Canonical Allele Identifier: PA2828327730
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 386725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Ala188Thr
CA10558543
NM_001369394.2:c.562G>A