Canonical Allele Identifier: PA2826955790
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1439710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Pro137Thr
CA415172537
NM_001316337.2:c.409C>A