Canonical Allele Identifier: PA2573180132
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1483849
ClinVar RCV Id: RCV002028145
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Ser10Thr
CA415301325
NM_001110792.2:c.29G>C