Canonical Allele Identifier: PA2826956038
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 158880

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Arg261Cys
CA206493
NM_001316337.2:c.781C>T