Canonical Allele Identifier: PA2825559274
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1906308
ClinVar RCV Id: RCV002586816
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Pro188Ala
CA415173876
NM_001110792.2:c.562C>G