Canonical Allele Identifier: PA2828327796
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143761

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Lys238Arg
CA170424
NM_001369394.2:c.713A>G