Canonical Allele Identifier: PA170280
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143509
ClinVar RCV Id: RCV000133040 RCV000981151 RCV001725999 RCV003380473
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Lys94Arg
CA170278
NM_001110792.2:c.281A>G