Canonical Allele Identifier: PA2829565061
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1189793
ClinVar RCV Id: RCV001550288 RCV002568315
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Pro176Ser
CA10558598
NM_004992.4:c.526C>T