Canonical Allele Identifier: PA2826955801
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 156670

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Ala141Gly
CA294719
NM_001316337.2:c.422C>G