Canonical Allele Identifier: PA2826955948
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143744
ClinVar RCV Id: RCV000133288
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Lys212Glu
CA270583
NM_001316337.2:c.634A>G