Canonical Allele Identifier: PA2825559239
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2613436
ClinVar RCV Id: RCV003373966

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Thr160Arg
CA415174787
NM_001110792.2:c.479C>G