ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA916047737
Gene: MECP2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
431705
ClinVar RCV Id:
RCV000655939
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001356323.1:p.Gly21_Ser23del
CA658799902
NM_001369394.2:c.62_70del