Canonical Allele Identifier: PA270368
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143546
ClinVar RCV Id: RCV000133079 RCV000254852
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Val134Met
CA270366
NM_001110792.2:c.400G>A