Canonical Allele Identifier: PA2826955634
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3066414
ClinVar RCV Id: RCV003991418
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Pro59Leu
CA415174704
NM_001316337.2:c.176C>T