ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2828325092
Gene: MECP2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
143569
ClinVar RCV Id:
RCV000133104
RCV001849959
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001356320.1:p.Tyr48Cys
CA270411
NM_001369391.2:c.143A>G