Canonical Allele Identifier: PA270427
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143580
ClinVar RCV Id: RCV000133117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Phe167Ile
CA270426
NM_001110792.2:c.499T>A