Canonical Allele Identifier: PA2828325039
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1331632
ClinVar RCV Id: RCV001806976

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Ala24_Gly25delinsSerTrp
CA2573055157
NM_001369391.2:c.70_73delinsTCCT