Canonical Allele Identifier: PA2829564987
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3024298
ClinVar RCV Id: RCV003883344
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Leu138Phe
CA415175141
NM_004992.4:c.414G>T
CA415175143
NM_004992.4:c.414G>C