Canonical Allele Identifier: PA280066
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 189760

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Asn138Ser
CA280064
NM_001110792.2:c.413A>G