Canonical Allele Identifier: PA2828327011
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143661

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Gly139Ala
CA170364
NM_001369393.2:c.416G>C