Canonical Allele Identifier: PA2829565808
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_004983.1:p.Pro480Leu
CA415163033
NM_004992.4:c.1439C>T