Canonical Allele Identifier: PA270569
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143735
ClinVar RCV Id: RCV000133278 RCV001067586 RCV001812116
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Pro314Ser
CA270567
NM_001110792.2:c.940C>T