Canonical Allele Identifier: PA270494
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143645
ClinVar RCV Id: RCV000133185
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.[Val224_Leu225del;Lys227_Lys231del]
CA270492
NM_001110792.2:c.671_691del