Canonical Allele Identifier: PA206494
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_004983.1:p.Arg354Cys
CA206493
NM_004992.4:c.1060C>T