Canonical Allele Identifier: PA916047762
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 11825

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Glu44Gly
CA121705
NM_001369394.2:c.131A>G