Canonical Allele Identifier: PA2828326851
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143580
ClinVar RCV Id: RCV000133117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Phe62Ile
CA270426
NM_001369393.2:c.184T>A