Canonical Allele Identifier: PA2573065353
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1325581

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.His380Tyr
CA10558509
NM_001110792.2:c.1138C>T