Canonical Allele Identifier: PA2826956363
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143477
ClinVar RCV Id: RCV000133007 RCV002055851 RCV003990983
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Pro387Ser
CA170251
NM_001316337.2:c.1159C>T