ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2828327851
Gene: MECP2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1325581
ClinVar RCV Id:
RCV001784168
RCV003638811
RCV004536310
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001356323.1:p.His275Tyr
CA10558509
NM_001369394.2:c.823C>T