Canonical Allele Identifier: PA2825559202
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1331632
ClinVar RCV Id: RCV001806976
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Ala129_Gly130delinsSerTrp
CA2573055157
NM_001110792.2:c.385_388delinsTCCT