Canonical Allele Identifier: PA2828325031
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 374353

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Arg18Lys
CA16043705
NM_001369391.2:c.53G>A