Canonical Allele Identifier: PA2829070022
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143488

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373068.1:p.Ser263_Ter264insLeuLeuTyrThrGluArgIleAlaLysGlnThrAsnLysAsnLysGlySerCysCysLeuPheSerLeuTrpValGlyLeu
CA232951
NM_001386139.1:c.791G>T