ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA270352
Gene: MECP2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
143535
ClinVar RCV Id:
RCV000133068
RCV001843481
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001104262.1:p.Arg118Leu
CA270350
NM_001110792.2:c.353G>T