Canonical Allele Identifier: PA916047818
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 156667
ClinVar RCV Id: RCV000144810 RCV000645120 RCV000680040
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Arg97Cys
CA294710
NM_001369394.2:c.289C>T