Canonical Allele Identifier: PA170292
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143547

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Val134Ala
CA170290
NM_001110792.2:c.401T>C