Canonical Allele Identifier: PA256088
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 11810
ClinVar RCV Id: RCV000012579
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Phe167Ser
CA256087
NM_001110792.2:c.500T>C