Canonical Allele Identifier: PA2828325092
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143569

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Tyr48Cys
CA270411
NM_001369391.2:c.143A>G