Canonical Allele Identifier: PA2828327763
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143742

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Lys211Glu
CA270580
NM_001369394.2:c.631A>G