Canonical Allele Identifier: PA2828325190
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143618

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Gly90Arg
CA170325
NM_001369391.2:c.268G>C
CA415173745
NM_001369391.2:c.268G>A