Canonical Allele Identifier: PA2573180133
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1376962
ClinVar RCV Id: RCV001889792
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Gly14Arg
CA415301152
NM_001110792.2:c.40G>C
CA415301157
NM_001110792.2:c.40G>A