Canonical Allele Identifier: PA2826955625
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2613436
ClinVar RCV Id: RCV003373966
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Thr55Arg
CA415174787
NM_001316337.2:c.164C>G