Canonical Allele Identifier: PA645400866
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 424578
ClinVar RCV Id: RCV000487257 RCV002525978 RCV001775123
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Arg97Cys
CA16621248
NM_001110792.2:c.289C>T