Canonical Allele Identifier: PA2826955563
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143545

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Asp28Gly
CA170287
NM_001316337.2:c.83A>G