Canonical Allele Identifier: PA2825559557
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143489
ClinVar RCV Id: RCV000133020

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Ser498_Ter499insCysLeuTyrThrGluArgIleAlaLysGlnThrAsnLysAsnLysGlySerCysCysLeuPheSerLeuTrpValGlyLeu
CA270292
NM_001110792.2:c.1497A>C
CA415162601
NM_001110792.2:c.1497A>T