Canonical Allele Identifier: PA2828327169
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143746

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Arg213His
CA270588
NM_001369393.2:c.638G>A