Canonical Allele Identifier: PA2826955800
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 211464
ClinVar RCV Id: RCV000194296
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Ala141Asp
CA208382
NM_001316337.2:c.422C>A