Canonical Allele Identifier: PA2826955752
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143637
ClinVar RCV Id: RCV000133177

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Gly113Asp
CA232987
NM_001316337.2:c.338G>A