Canonical Allele Identifier: PA2580229870
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2028633
ClinVar RCV Id: RCV002876235
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Ala38Pro
CA415175357
NM_001369394.2:c.112G>C