Canonical Allele Identifier: PA294700
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 156663
ClinVar RCV Id: RCV000144806 RCV002055865 RCV002514780
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Val58Met
CA294698
NM_001110792.2:c.172G>A