Canonical Allele Identifier: PA206495
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 158880
ClinVar RCV Id: RCV000193184 RCV000724672 RCV001432219 RCV002472366
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Arg366Cys
CA206493
NM_001110792.2:c.1096C>T