Canonical Allele Identifier: PA222803
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 95190

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Ala451Ser
CA222801
NM_001110792.2:c.1351G>T