ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826955568
Gene: MECP2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
143549
ClinVar RCV Id:
RCV000133082
ClinVar Variation Id:
143550
ClinVar RCV Id:
RCV000133083
RCV001383621
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001303266.1:p.Leu31Phe
CA270369
NM_001316337.2:c.93G>C
CA270371
NM_001316337.2:c.93G>T