ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2828326117
Gene: MECP2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1678856
ClinVar RCV Id:
RCV002226170
RCV003089209
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001356321.1:p.Leu120Val
CA10558575
NM_001369392.2:c.358C>G