Canonical Allele Identifier: PA658802926
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 431705
ClinVar RCV Id: RCV000655939

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Gly126_Ser128del
CA658799902
NM_001110792.2:c.377_385del