Canonical Allele Identifier: PA2829069282
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1325581

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373067.1:p.His145Tyr
CA10558509
NM_001386138.1:c.433C>T