Canonical Allele Identifier: PA121706
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 11825
ClinVar RCV Id: RCV000012598 RCV001230698 RCV001566839
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Glu149Gly
CA121705
NM_001110792.2:c.446A>G