Canonical Allele Identifier: PA270439
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143590
ClinVar RCV Id: RCV000133128 RCV000482544 RCV003522933
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Thr170Ala
CA270438
NM_001110792.2:c.508A>G