Canonical Allele Identifier: PA1139673389
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 940151
ClinVar RCV Id: RCV001209680
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Pro211Leu
CA415173153
NM_001110792.2:c.632C>T