Canonical Allele Identifier: PA2828327980
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 279847

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Glu390Lys
CA10603533
NM_001369394.2:c.1168G>A