Canonical Allele Identifier: PA2573210954
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1405732
ClinVar RCV Id: RCV001906666
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Lys14Arg
CA415176830
NM_001369394.2:c.41A>G