Canonical Allele Identifier: PA2499238005
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1003411
ClinVar RCV Id: RCV001299959
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Val497Leu
CA10558426
NM_001110792.2:c.1489G>C