Canonical Allele Identifier: PA2825559208
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1506669
ClinVar RCV Id: RCV002006896

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Leu136Val
CA415176431
NM_001110792.2:c.406T>G