Allele Registry

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Canonical Allele Identifier: PA294718

Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 156669

ClinVar RCV Id: RCV000726052 RCV000718449 RCV002265623 RCV002472364 RCV002514781 RCV004532634

ClinVar Variation Id: 2845786

ClinVar RCV Id: RCV003640178

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001104262.1:p.Gly243Arg	CA294716 NM_001110792.2:c.727G>A CA415172511 NM_001110792.2:c.727G>C