Canonical Allele Identifier: PA916047732
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143536
ClinVar RCV Id: RCV000133069

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Leu15His
CA270353
NM_001369394.2:c.44T>A