Canonical Allele Identifier: PA916047807
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143611

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Pro83Arg
CA170319
NM_001369394.2:c.248C>G