Canonical Allele Identifier: PA2829069560
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143490

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373067.1:p.Ser263_Ter264insTrpLeuTyrThrGluArgIleAlaLysGlnThrAsnLysAsnLysGlySerCysCysLeuPheSerLeuTrpValGlyLeu
CA170257
NM_001386138.1:c.792A>G