Canonical Allele Identifier: PA2829565820
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143489
ClinVar RCV Id: RCV000133020

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Ser486_Ter487insCysLeuTyrThrGluArgIleAlaLysGlnThrAsnLysAsnLysGlySerCysCysLeuPheSerLeuTrpValGlyLeu
CA270292
NM_004992.4:c.1461A>C
CA415162601
NM_004992.4:c.1461A>T