Canonical Allele Identifier: PA2826955799
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143661

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Gly139Ala
CA170364
NM_001316337.2:c.416G>C