Canonical Allele Identifier: PA170348
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143638
ClinVar RCV Id: RCV000133178 RCV000457783 RCV001711300 RCV002472327
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Gly218Ala
CA170346
NM_001110792.2:c.653G>C