Canonical Allele Identifier: PA2825559258
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1494485
ClinVar RCV Id: RCV002015021
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Pro177Ser
CA415174257
NM_001110792.2:c.529C>T