Canonical Allele Identifier: PA645400918
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 374353

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Arg123Lys
CA16043705
NM_001110792.2:c.368G>A