Canonical Allele Identifier: PA2825559269
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 928877

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Pro184Thr
CA415173983
NM_001110792.2:c.550C>A