Canonical Allele Identifier: PA2828325100
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 189627

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Lys51Arg
CA199462
NM_001369391.2:c.152A>G