Canonical Allele Identifier: PA2829565084
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 566728

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Arg188Trp
CA10558590
NM_004992.4:c.562C>T