Canonical Allele Identifier: PA916047738
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143540
ClinVar RCV Id: RCV000133073
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Gly21Ala
CA270359
NM_001369394.2:c.62G>C