Canonical Allele Identifier: PA2825559288
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2117601
ClinVar RCV Id: RCV003027825

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Gly197Cys
CA415173667
NM_001110792.2:c.589G>T