Canonical Allele Identifier: PA2825559249
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2711943
ClinVar RCV Id: RCV003524291
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Phe169Cys
CA415174551
NM_001110792.2:c.506T>G