Canonical Allele Identifier: PA270450
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143598

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Gly173Val
CA270449
NM_001110792.2:c.518G>T