Allele Registry

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Canonical Allele Identifier: PA170262

Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143493

ClinVar RCV Id: RCV000133024 RCV003483516 RCV001857482

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001104262.1:p.His63Gln	CA170260 NM_001110792.2:c.189C>G CA415177857 NM_001110792.2:c.189C>A