ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826955591
Gene: MECP2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
11809
ClinVar RCV Id:
RCV000012578
RCV000030666
RCV000081202
RCV000170107
RCV000169934
RCV000445570
RCV000460141
RCV000624907
RCV001257757
RCV002273925
RCV003984804
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001303266.1:p.Arg40Cys
CA211250
NM_001316337.2:c.118C>T