Canonical Allele Identifier: PA170350
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143644
ClinVar RCV Id: RCV000133184 RCV000645121 RCV001719907 RCV002354329 RCV003380478 RCV004532607
ClinVar Variation Id: 1135970
ClinVar RCV Id: RCV001471449
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Arg211Ser
CA170349
NM_004992.4:c.633G>C
CA415172926
NM_004992.4:c.633G>T