Canonical Allele Identifier: PA2829069026
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 211466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373067.1:p.Arg27Cys
CA205183
NM_001386138.1:c.79C>T