Canonical Allele Identifier: PA916047766
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143569

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Tyr48Cys
CA270411
NM_001369394.2:c.143A>G