Canonical Allele Identifier: PA2741830571
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2839997
ClinVar RCV Id: RCV003640098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Pro492Leu
CA415163033
NM_001110792.2:c.1475C>T