Canonical Allele Identifier: PA2825559315
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1439710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Pro242Thr
CA415172537
NM_001110792.2:c.724C>A