Canonical Allele Identifier: PA170411
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_001104262.1:p.Thr323Met
CA170409
NM_001110792.2:c.968C>T