Canonical Allele Identifier: PA2829070019
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1003411
ClinVar RCV Id: RCV001299959
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373068.1:p.Val262Leu
CA10558426
NM_001386139.1:c.784G>C