Canonical Allele Identifier: PA658694609
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 496278
ClinVar RCV Id: RCV000587702
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Ala91Ser
CA415177391
NM_001110792.2:c.271G>T