Canonical Allele Identifier: PA274627
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143526
ClinVar RCV Id: RCV000133058 RCV000170238 RCV001857483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Pro113Arg
CA274626
NM_001110792.2:c.338C>G