Canonical Allele Identifier: PA916047777
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143580
ClinVar RCV Id: RCV000133117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Phe62Ile
CA270426
NM_001369394.2:c.184T>A