Canonical Allele Identifier: PA170264
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143494
ClinVar RCV Id: RCV000133025 RCV001520931 RCV001689675 RCV002472326
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.His52Arg
CA170263
NM_004992.4:c.155A>G