Canonical Allele Identifier: PA232925
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143418

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Pro405Leu
CA232923
NM_001110792.2:c.1214C>T