Canonical Allele Identifier: PA2828325640
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Pro298del
CA232908
NM_001369391.2:c.882_884del
CA1138553958
NM_001369391.2:c.885_887del
CA2695100356
NM_001369391.2:c.891_893del
CA2695100362
NM_001369391.2:c.888_890del