Canonical Allele Identifier: PA170247
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143475
ClinVar RCV Id: RCV000133005 RCV001206116 RCV001800448
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Ser489Thr
CA170245
NM_001110792.2:c.1466G>C