Canonical Allele Identifier: PA2829070017
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143483

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373068.1:p.Arg261Thr
CA172565
NM_001386139.1:c.782G>C