Canonical Allele Identifier: PA658802942
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 508389
ClinVar RCV Id: RCV000605015
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Leu233Val
CA415172759
NM_001110792.2:c.697C>G