Canonical Allele Identifier: PA2741873910
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2687738
ClinVar RCV Id: RCV003484978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Asn33Ile
CA415176375
NM_001369394.2:c.98A>T