Canonical Allele Identifier: PA2828327636
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 851266

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Ala109Gly
CA415173087
NM_001369394.2:c.326C>G