Canonical Allele Identifier: PA645401232
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 290402
ClinVar RCV Id: RCV000361062 RCV002522026
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Val219Ala
CA10606762
NM_001110792.2:c.656T>C