Canonical Allele Identifier: PA891861429
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 566728

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Arg200Trp
CA10558590
NM_001110792.2:c.598C>T