Canonical Allele Identifier: PA658802910
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 517006

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Gly16del
CA10558690
NM_001110792.2:c.45_47del
CA2695105432
NM_001110792.2:c.47_49del