Canonical Allele Identifier: PA2826956380
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143488

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Ser393_Ter394insLeuLeuTyrThrGluArgIleAlaLysGlnThrAsnLysAsnLysGlySerCysCysLeuPheSerLeuTrpValGlyLeu
CA232951
NM_001316337.2:c.1181G>T