Canonical Allele Identifier: PA2829069694
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143317

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373068.1:p.Arg131Leu
CA170157
NM_001386139.1:c.392G>T