Canonical Allele Identifier: PA270386
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143556

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Ala143Asp
CA270384
NM_001110792.2:c.428C>A