Canonical Allele Identifier: PA891861438
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 565838
ClinVar RCV Id: RCV001416199
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Val224Phe
CA415172923
NM_001110792.2:c.670G>T