ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826955608
Gene: MECP2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
11823
ClinVar RCV Id:
RCV000012596
RCV000020628
RCV000224266
RCV000414791
RCV000544176
RCV001004016
RCV001374894
RCV001197458
RCV001257756
RCV001249626
RCV002326676
RCV002466399
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001303266.1:p.Ala47Val
CA121703
NM_001316337.2:c.140C>T