Canonical Allele Identifier: PA2741873908
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2505626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Arg22His
CA10558640
NM_001369394.2:c.65G>A