Canonical Allele Identifier: PA2826955589
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1679147
ClinVar RCV Id: RCV002226590
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Arg40Pro
CA415175270
NM_001316337.2:c.119G>C