Canonical Allele Identifier: PA270352
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Arg118Leu
CA270350
NM_001110792.2:c.353G>T