Canonical Allele Identifier: PA2573180142
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1397676
ClinVar RCV Id: RCV001912577
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Gln31Glu
CA415178943
NM_001110792.2:c.91C>G