Canonical Allele Identifier: PA2828328081
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143733
ClinVar RCV Id: RCV000133276
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Pro209Thr
CA270562
NM_001369394.2:c.625C>A