Canonical Allele Identifier: PA2829565027
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1992323
ClinVar RCV Id: RCV002795901

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Thr160Asn
CA415174434
NM_004992.4:c.479C>A