Canonical Allele Identifier: PA2828327591
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143489
ClinVar RCV Id: RCV000133020

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Ser393_Ter394insCysLeuTyrThrGluArgIleAlaLysGlnThrAsnLysAsnLysGlySerCysCysLeuPheSerLeuTrpValGlyLeu
CA270292
NM_001369393.2:c.1182A>C
CA415162601
NM_001369393.2:c.1182A>T