ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA121714
Gene: MECP2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
11841
ClinVar RCV Id:
RCV000012615
RCV000133194
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001104262.1:p.Pro237Leu
CA121713
NM_001110792.2:c.710C>T