Canonical Allele Identifier: PA270385
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143556

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Ala131Asp
CA270384
NM_004992.4:c.392C>A