Canonical Allele Identifier: PA2580145050
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2132914
ClinVar RCV Id: RCV003063909
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Lys47Glu
CA415178434
NM_001110792.2:c.139A>G