Canonical Allele Identifier: PA645401139
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406154
ClinVar RCV Id: RCV000467894 RCV002244934
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Pro188Leu
CA16616643
NM_001110792.2:c.563C>T