Canonical Allele Identifier: PA2826955557
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_001303266.1:p.Ala24_Gly25delinsSerTrp
CA2573055157
NM_001316337.2:c.70_73delinsTCCT