Canonical Allele Identifier: PA2829565063
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_004983.1:p.Pro176Ala
CA415173876
NM_004992.4:c.526C>G