Canonical Allele Identifier: PA2829068692
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1325581

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373066.1:p.His145Tyr
CA10558509
NM_001386137.1:c.433C>T