Canonical Allele Identifier: PA2829069992
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2848886
ClinVar RCV Id: RCV003640217
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373068.1:p.Pro246Leu
CA415163451
NM_001386139.1:c.737C>T