Canonical Allele Identifier: PA270375
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143552

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Pro139Leu
CA270373
NM_001110792.2:c.416C>T