Canonical Allele Identifier: PA170238
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143465
ClinVar RCV Id: RCV000132993 RCV000678237 RCV001088957 RCV001800447 RCV004544311 RCV002381448
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Ala459Thr
CA170236
NM_001110792.2:c.1375G>A