Canonical Allele Identifier: PA2829069821
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_001373068.1:p.Pro168del
CA1138553958
NM_001386139.1:c.495_497del
CA2695100356
NM_001386139.1:c.501_503del
CA2695100362
NM_001386139.1:c.498_500del