Canonical Allele Identifier: PA2828326922
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143618

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Gly90Arg
CA170325
NM_001369393.2:c.268G>C
CA415173745
NM_001369393.2:c.268G>A