Canonical Allele Identifier: PA2580145052
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2105763
ClinVar RCV Id: RCV003023622
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Gly72Ser
CA415177654
NM_001110792.2:c.214G>A