Canonical Allele Identifier: PA2826955523
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1324711
ClinVar RCV Id: RCV001782431

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Pro8Thr
CA415176913
NM_001316337.2:c.22C>A