ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826955657
Gene: MECP2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
143598
ClinVar RCV Id:
RCV000133137
RCV003522934
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001303266.1:p.Gly68Val
CA270449
NM_001316337.2:c.203G>T