Canonical Allele Identifier: PA2825559247
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 804127
ClinVar RCV Id: RCV000991002
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Asp168Tyr
CA415174595
NM_001110792.2:c.502G>T