Canonical Allele Identifier: PA916047780
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 95196
ClinVar Variation Id: 393489
ClinVar RCV Id: RCV000445574

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Asp63Glu
CA202769
NM_001369394.2:c.189C>G
CA16609353
NM_001369394.2:c.189C>A