Canonical Allele Identifier: PA645401721
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 378124

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Arg483Thr
CA16609147
NM_001110792.2:c.1448G>C