Canonical Allele Identifier: PA208888
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 36492
ClinVar RCV Id: RCV000030164 RCV000194612 RCV000724867 RCV001057144
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Val493Met
CA208886
NM_001110792.2:c.1477G>A