Canonical Allele Identifier: PA170365
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143661

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Gly232Ala
CA170364
NM_004992.4:c.695G>C