Canonical Allele Identifier: PA2829068765
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373066.1:p.Pro168del
CA232908
NM_001386137.1:c.492_494del
CA1138553958
NM_001386137.1:c.495_497del
CA2695100356
NM_001386137.1:c.501_503del
CA2695100362
NM_001386137.1:c.498_500del