Canonical Allele Identifier: PA916047769
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 189627

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Lys51Arg
CA199462
NM_001369394.2:c.152A>G