Canonical Allele Identifier: PA916047791
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143598

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Gly68Val
CA270449
NM_001369394.2:c.203G>T