Canonical Allele Identifier: PA170274
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143504
ClinVar RCV Id: RCV000133035 RCV000195208 RCV001414793 RCV004532599 RCV002515929
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Pro87Leu
CA170272
NM_001110792.2:c.260C>T