Canonical Allele Identifier: PA916047742
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143545

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Asp28Gly
CA170287
NM_001369394.2:c.83A>G