Canonical Allele Identifier: PA2828327639
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143638

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Gly113Ala
CA170346
NM_001369394.2:c.338G>C