Canonical Allele Identifier: PA916047771
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 717385
ClinVar RCV Id: RCV000890166 RCV002332859
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Thr55Ala
CA415174791
NM_001369394.2:c.163A>G