Canonical Allele Identifier: PA2828326727
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143487

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356321.1:p.Ser393_Ter394insArgLeuTyrThrGluArgIleAlaLysGlnThrAsnLysAsnLysGlySerCysCysLeuPheSerLeuTrpValGlyLeu
CA232948
NM_001369392.2:c.1180T>C
CA415162673
NM_001369392.2:c.1180T>A