Canonical Allele Identifier: PA645400631
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143521
ClinVar RCV Id: RCV000133052
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Thr99del
CA270325
NM_004992.4:c.295_297del