Canonical Allele Identifier: PA2826956036
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143317

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Arg261Leu
CA170157
NM_001316337.2:c.782G>T