Canonical Allele Identifier: PA1139742539
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 995700
ClinVar RCV Id: RCV001810713
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Asp28Glu
CA415176488
NM_001369394.2:c.84T>A
CA415176490
NM_001369394.2:c.84T>G