Canonical Allele Identifier: PA2828328190
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143389
ClinVar RCV Id: RCV000132915 RCV000602397 RCV003638623
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Pro298del
CA1138553958
NM_001369394.2:c.885_887del
CA2695100356
NM_001369394.2:c.891_893del
CA2695100362
NM_001369394.2:c.888_890del