Canonical Allele Identifier: PA2825559270
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 804125

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Pro185Thr
CA415173958
NM_001110792.2:c.553C>A