Canonical Allele Identifier: PA1139673234
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 969689
ClinVar RCV Id: RCV001245089

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Ala8Glu
CA415301470
NM_001110792.2:c.23C>A