Canonical Allele Identifier: PA270539
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143716

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Ala287Pro
CA270538
NM_004992.4:c.859G>C