Canonical Allele Identifier: PA2573078764
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 36496
ClinVar RCV Id: RCV000030168 RCV000133294 RCV000426076 RCV000712288 RCV001089108 RCV002316203 RCV004541029
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373068.1:p.Thr88Met
CA170409
NM_001386139.1:c.263C>T